Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 145773 |
|---|---|
| ensemblid | ENSG00000157470.12 |
| hgncid | 28379 |
| symbol | FAM81A |
| name | family with sequence similarity 81 member A |
| refseq_nuc | NM_152450.3 |
| refseq_prot | NP_689663.2 |
| ensembl_nuc | ENST00000288228.10 |
| ensembl_prot | ENSP00000288228.5 |
| mane_status | MANE Select |
| chr | chr15 |
| start | 59438186 |
| end | 59523555 |
| strand | + |
| ver | v1.2 |
| region | chr15:59438186-59523555 |
| region5000 | chr15:59433186-59528555 |
| regionname0 | FAM81A_chr15_59438186_59523555 |
| regionname5000 | FAM81A_chr15_59433186_59528555 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 368 | 370 | 90 | 65 | 162 | 12 | 39 | 124 | FAM81A_chr15_59433186_59528555 | FAM81A | copy fasta | chr15 | 59433186 | 59528555 |
| a0002 | 0/0 | 368 | 2 | 0 | 1 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | copy fasta | chr15 | 59433186 | 59528555 |
| a0003 | 0/0 | 368 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | copy fasta | chr15 | 59433186 | 59528555 |
| a0004 | 0/0 | 368 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | copy fasta | chr15 | 59433186 | 59528555 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/1 | 1107 | 284 | 51 | 58 | 135 | 8 | 31 | FAM81A_chr15_59433186_59528555 | FAM81A | copy fasta | chr15 | 59433186 | 59528555 |
| c0002 | 1/0 | 1107 | 81 | 34 | 7 | 27 | 4 | 8 | FAM81A_chr15_59433186_59528555 | FAM81A | copy fasta | chr15 | 59433186 | 59528555 |
| c0003 | 0/0 | 1107 | 4 | 4 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | copy fasta | chr15 | 59433186 | 59528555 |
| c0004 | 0/0 | 1107 | 1 | 0 | 0 | 0 | 1 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | copy fasta | chr15 | 59433186 | 59528555 |
| c0005 | 0/0 | 1107 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | copy fasta | chr15 | 59433186 | 59528555 |
| c0006 | 0/0 | 1107 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81A_chr15_59433186_59528555 | FAM81A | copy fasta | chr15 | 59433186 | 59528555 |
| c0007 | 0/0 | 1107 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | copy fasta | chr15 | 59433186 | 59528555 |
| c0008 | 0/0 | 1107 | 1 | 0 | 0 | 0 | 1 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | copy fasta | chr15 | 59433186 | 59528555 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 2352 | 326 | 57 | 64 | 154 | 11 | 38 | FAM81A_chr15_59433186_59528555 | FAM81A | copy fasta | chr15 | 59433186 | 59528555 |
| t0002 | 0/0 | 2352 | 7 | 7 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | copy fasta | chr15 | 59433186 | 59528555 |
| t0003 | 0/0 | 2352 | 7 | 7 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | copy fasta | chr15 | 59433186 | 59528555 |
| t0004 | 0/0 | 2352 | 6 | 1 | 1 | 1 | 2 | 1 | FAM81A_chr15_59433186_59528555 | FAM81A | copy fasta | chr15 | 59433186 | 59528555 |
| t0005 | 0/0 | 2352 | 6 | 6 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | copy fasta | chr15 | 59433186 | 59528555 |
| t0006 | 0/0 | 2352 | 3 | 0 | 0 | 3 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | copy fasta | chr15 | 59433186 | 59528555 |
| t0007 | 0/0 | 2352 | 3 | 3 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | copy fasta | chr15 | 59433186 | 59528555 |
| t0008 | 0/0 | 2352 | 2 | 0 | 0 | 2 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | copy fasta | chr15 | 59433186 | 59528555 |
| t0009 | 0/0 | 2352 | 2 | 0 | 1 | 0 | 1 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | copy fasta | chr15 | 59433186 | 59528555 |
| t0010 | 0/0 | 2352 | 2 | 2 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | copy fasta | chr15 | 59433186 | 59528555 |
| t0011 | 0/0 | 2352 | 2 | 2 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | copy fasta | chr15 | 59433186 | 59528555 |
| t0012 | 0/0 | 2352 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | copy fasta | chr15 | 59433186 | 59528555 |
| t0013 | 0/0 | 2352 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | copy fasta | chr15 | 59433186 | 59528555 |
| t0014 | 0/0 | 2352 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | copy fasta | chr15 | 59433186 | 59528555 |
| t0015 | 0/0 | 2352 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | copy fasta | chr15 | 59433186 | 59528555 |
| t0016 | 0/0 | 2366 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | copy fasta | chr15 | 59433186 | 59528555 |
| t0017 | 0/0 | 2352 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81A_chr15_59433186_59528555 | FAM81A | copy fasta | chr15 | 59433186 | 59528555 |
| t0018 | 0/0 | 2352 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | copy fasta | chr15 | 59433186 | 59528555 |
| t0019 | 0/0 | 2352 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | copy fasta | chr15 | 59433186 | 59528555 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0003 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0006 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0009 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0238 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0309 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0329 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0332 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0341 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0348 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0352 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1107 | 284 | 51 | 58 | 135 | 8 | 31 | FAM81A_chr15_59433186_59528555 | FAM81A | copy fasta | chr15 | 59433186 | 59528555 |
| a0001c0002 | 1/0 | 1107 | 81 | 34 | 7 | 27 | 4 | 8 | FAM81A_chr15_59433186_59528555 | FAM81A | copy fasta | chr15 | 59433186 | 59528555 |
| a0001c0003 | 0/0 | 1107 | 4 | 4 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | copy fasta | chr15 | 59433186 | 59528555 |
| a0001c0005 | 0/0 | 1107 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | copy fasta | chr15 | 59433186 | 59528555 |
| a0002c0004 | 0/0 | 1107 | 1 | 0 | 0 | 0 | 1 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | copy fasta | chr15 | 59433186 | 59528555 |
| a0002c0007 | 0/0 | 1107 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | copy fasta | chr15 | 59433186 | 59528555 |
| a0003c0006 | 0/0 | 1107 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81A_chr15_59433186_59528555 | FAM81A | copy fasta | chr15 | 59433186 | 59528555 |
| a0004c0008 | 0/0 | 1107 | 1 | 0 | 0 | 0 | 1 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | copy fasta | chr15 | 59433186 | 59528555 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 3458 | 278 | 50 | 57 | 133 | 7 | 30 | FAM81A_chr15_59433186_59528555 | FAM81A | copy fasta | chr15 | 59433186 | 59528555 |
| a0001c0001t0009 | 0/0 | 3458 | 2 | 0 | 1 | 0 | 1 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | copy fasta | chr15 | 59433186 | 59528555 |
| a0001c0001t0016 | 0/0 | 3472 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | copy fasta | chr15 | 59433186 | 59528555 |
| a0001c0001t0017 | 0/0 | 3458 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81A_chr15_59433186_59528555 | FAM81A | copy fasta | chr15 | 59433186 | 59528555 |
| a0001c0001t0018 | 0/0 | 3458 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | copy fasta | chr15 | 59433186 | 59528555 |
| a0001c0001t0019 | 0/0 | 3458 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | copy fasta | chr15 | 59433186 | 59528555 |
| a0001c0002t0001 | 1/0 | 3458 | 45 | 7 | 6 | 21 | 3 | 7 | FAM81A_chr15_59433186_59528555 | FAM81A | copy fasta | chr15 | 59433186 | 59528555 |
| a0001c0002t0002 | 0/0 | 3458 | 2 | 2 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | copy fasta | chr15 | 59433186 | 59528555 |
| a0001c0002t0003 | 0/0 | 3458 | 7 | 7 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | copy fasta | chr15 | 59433186 | 59528555 |
| a0001c0002t0004 | 0/0 | 3458 | 5 | 1 | 1 | 1 | 1 | 1 | FAM81A_chr15_59433186_59528555 | FAM81A | copy fasta | chr15 | 59433186 | 59528555 |
| a0001c0002t0005 | 0/0 | 3458 | 6 | 6 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | copy fasta | chr15 | 59433186 | 59528555 |
| a0001c0002t0006 | 0/0 | 3458 | 3 | 0 | 0 | 3 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | copy fasta | chr15 | 59433186 | 59528555 |
| a0001c0002t0007 | 0/0 | 3458 | 3 | 3 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | copy fasta | chr15 | 59433186 | 59528555 |
| a0001c0002t0008 | 0/0 | 3458 | 2 | 0 | 0 | 2 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | copy fasta | chr15 | 59433186 | 59528555 |
| a0001c0002t0010 | 0/0 | 3458 | 2 | 2 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | copy fasta | chr15 | 59433186 | 59528555 |
| a0001c0002t0011 | 0/0 | 3458 | 2 | 2 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | copy fasta | chr15 | 59433186 | 59528555 |
| a0001c0002t0012 | 0/0 | 3458 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | copy fasta | chr15 | 59433186 | 59528555 |
| a0001c0002t0013 | 0/0 | 3458 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | copy fasta | chr15 | 59433186 | 59528555 |
| a0001c0002t0014 | 0/0 | 3458 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | copy fasta | chr15 | 59433186 | 59528555 |
| a0001c0002t0015 | 0/0 | 3458 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | copy fasta | chr15 | 59433186 | 59528555 |
| a0001c0003t0002 | 0/0 | 3458 | 4 | 4 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | copy fasta | chr15 | 59433186 | 59528555 |
| a0001c0005t0002 | 0/0 | 3458 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | copy fasta | chr15 | 59433186 | 59528555 |
| a0002c0004t0004 | 0/0 | 3458 | 1 | 0 | 0 | 0 | 1 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | copy fasta | chr15 | 59433186 | 59528555 |
| a0002c0007t0001 | 0/0 | 3458 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | copy fasta | chr15 | 59433186 | 59528555 |
| a0003c0006t0001 | 0/0 | 3458 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81A_chr15_59433186_59528555 | FAM81A | copy fasta | chr15 | 59433186 | 59528555 |
| a0004c0008t0001 | 0/0 | 3458 | 1 | 0 | 0 | 0 | 1 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | copy fasta | chr15 | 59433186 | 59528555 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0329 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0341 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0348 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0352 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0001g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0009g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0009g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0016g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0017g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0018g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0001t0019g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0002t0001g0001 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0002t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0002t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0002t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0002t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0002t0001g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0002t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0002t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0002t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0002t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0002t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0002t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0002t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0002t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0002t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0002t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0002t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0002t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0002t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0002t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0002t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0002t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0002t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0002t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0002t0001g0238 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0002t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0002t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0002t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0002t0001g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0002t0001g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0002t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0002t0002g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0002t0003g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0002t0003g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0002t0003g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0002t0003g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0002t0003g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0002t0003g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0002t0003g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0002t0004g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0002t0004g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0002t0004g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0002t0004g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0002t0004g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0002t0005g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0002t0005g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0002t0005g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0002t0005g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0002t0005g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0002t0005g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0002t0006g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0002t0006g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0002t0006g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0002t0007g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0002t0007g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0002t0007g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0002t0008g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0002t0008g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0002t0010g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0002t0010g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0002t0011g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0002t0012g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0002t0013g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0002t0014g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0002t0015g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0003t0002g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0003t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0003t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0001c0005t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0002c0004t0004g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0002c0007t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0003c0006t0001g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| a0004c0008t0001g0309 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0001 | g0041 | EUR | GBR | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0097 | EUR | GBR | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0120 | EUR | FIN | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG00323 | hp2 | a0004 | c0008 | t0001 | g0309 | EUR | FIN | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0346 | EAS | CHS | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | CHS | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG00438 | hp1 | a0001 | c0002 | t0001 | g0298 | EAS | CHS | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | CHS | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | CHS | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | CHS | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | CHS | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | CHS | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | CHS | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0300 | EAS | CHS | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG00642 | hp1 | a0001 | c0002 | t0001 | g0023 | AMR | PUR | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | PUR | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | CHS | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG00673 | hp2 | a0001 | c0002 | t0001 | g0018 | EAS | CHS | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0181 | AMR | PUR | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG00738 | hp2 | a0001 | c0002 | t0001 | g0029 | AMR | PUR | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | PUR | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0335 | AMR | PUR | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0333 | AMR | PUR | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0334 | AMR | PUR | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0319 | AMR | PUR | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG01109 | hp1 | a0001 | c0002 | t0004 | g0244 | AMR | PUR | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0230 | AMR | PUR | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | PUR | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0331 | AMR | PUR | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | PUR | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0343 | AMR | PUR | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | PUR | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0231 | AMR | PUR | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | CLM | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | CLM | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0202 | AMR | CLM | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG01257 | hp2 | a0001 | c0002 | t0001 | g0033 | AMR | CLM | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG01258 | hp1 | a0001 | c0002 | t0001 | g0034 | AMR | CLM | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | CLM | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG01261 | hp1 | a0002 | c0007 | t0001 | g0177 | AMR | CLM | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | CLM | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | CLM | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0189 | AMR | CLM | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | CLM | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0045 | AMR | CLM | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0176 | AMR | CLM | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG01361 | hp2 | a0001 | c0001 | t0009 | g0132 | AMR | CLM | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | CLM | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0216 | AMR | CLM | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | CLM | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0332 | EUR | IBS | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG01515 | hp2 | a0001 | c0002 | t0001 | g0036 | EUR | IBS | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0093 | EUR | IBS | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG01516 | hp2 | a0002 | c0004 | t0004 | g0253 | EUR | IBS | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0106 | EUR | IBS | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG01517 | hp2 | a0001 | c0002 | t0001 | g0035 | EUR | IBS | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | ACB | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG01884 | hp2 | a0001 | c0002 | t0003 | g0143 | AFR | ACB | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG01891 | hp1 | a0001 | c0002 | t0001 | g0011 | AFR | ACB | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | ACB | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | PEL | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0195 | AMR | PEL | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | PEL | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0347 | AMR | PEL | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0209 | AMR | PEL | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0295 | AMR | PEL | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0311 | AMR | PEL | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG01978 | hp2 | a0001 | c0002 | t0001 | g0053 | AMR | PEL | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0289 | AMR | PEL | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG01993 | hp2 | a0001 | c0002 | t0001 | g0056 | AMR | PEL | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0315 | AMR | PEL | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | KHV | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG02015 | hp2 | a0001 | c0002 | t0001 | g0048 | EAS | KHV | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | KHV | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | KHV | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0336 | AFR | ACB | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG02055 | hp2 | a0001 | c0002 | t0001 | g0026 | AFR | ACB | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | KHV | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | KHV | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | KHV | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | KHV | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | KHV | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG02074 | hp2 | a0001 | c0002 | t0001 | g0127 | EAS | KHV | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0305 | EAS | KHV | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | KHV | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | KHV | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | KHV | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | KHV | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0360 | EAS | KHV | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG02132 | hp2 | a0001 | c0001 | t0016 | g0166 | EAS | KHV | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | KHV | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | KHV | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0234 | AFR | ACB | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0265 | AFR | ACB | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0194 | AMR | PEL | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | PEL | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | CDX | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | CDX | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0237 | AFR | ACB | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | ACB | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG02258 | hp1 | a0001 | c0002 | t0005 | g0236 | AFR | ACB | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0326 | AFR | ACB | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0354 | AMR | PEL | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0233 | AFR | ACB | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0226 | AFR | ACB | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0267 | AFR | ACB | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG02451 | hp2 | a0001 | c0002 | t0003 | g0139 | AFR | ACB | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | KHV | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | KHV | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0279 | SAS | PJL | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG02602 | hp2 | a0001 | c0002 | t0001 | g0021 | SAS | PJL | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG02615 | hp1 | a0001 | c0002 | t0003 | g0142 | AFR | GWD | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG02615 | hp2 | a0001 | c0002 | t0001 | g0350 | AFR | GWD | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG02622 | hp1 | a0001 | c0003 | t0002 | g0004 | AFR | GWD | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | GWD | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG02630 | hp1 | a0001 | c0005 | t0002 | g0049 | AFR | GWD | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0288 | AFR | GWD | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG02647 | hp1 | a0001 | c0002 | t0004 | g0015 | AFR | GWD | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | GWD | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0055 | SAS | PJL | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0348 | SAS | PJL | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG02698 | hp1 | a0001 | c0002 | t0001 | g0031 | SAS | PJL | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0341 | SAS | PJL | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG02723 | hp1 | a0001 | c0002 | t0005 | g0276 | AFR | GWD | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | GWD | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG02735 | hp1 | a0001 | c0002 | t0004 | g0247 | SAS | PJL | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0107 | SAS | PJL | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG02809 | hp1 | a0001 | c0002 | t0001 | g0224 | AFR | GWD | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG02809 | hp2 | a0001 | c0002 | t0005 | g0359 | AFR | GWD | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0337 | AFR | GWD | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0355 | AFR | GWD | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | GWD | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG02886 | hp2 | a0001 | c0002 | t0005 | g0275 | AFR | GWD | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG02895 | hp1 | a0001 | c0002 | t0001 | g0135 | AFR | GWD | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0356 | AFR | GWD | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG02896 | hp1 | a0001 | c0002 | t0003 | g0271 | AFR | GWD | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG02896 | hp2 | a0001 | c0003 | t0002 | g0051 | AFR | GWD | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG02897 | hp1 | a0001 | c0002 | t0001 | g0136 | AFR | GWD | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG02897 | hp2 | a0001 | c0003 | t0002 | g0052 | AFR | GWD | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG02922 | hp1 | a0001 | c0002 | t0015 | g0227 | AFR | ESN | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG02922 | hp2 | a0001 | c0003 | t0002 | g0004 | AFR | ESN | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0363 | AFR | ESN | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0328 | AFR | ESN | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | ESN | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG02970 | hp2 | a0001 | c0002 | t0011 | g0010 | AFR | ESN | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | ESN | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | ESN | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG03017 | hp1 | a0001 | c0001 | t0017 | g0220 | SAS | PJL | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0173 | SAS | PJL | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | GWD | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0338 | AFR | GWD | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG03098 | hp1 | a0001 | c0002 | t0010 | g0257 | AFR | MSL | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0235 | AFR | MSL | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG03130 | hp1 | a0001 | c0002 | t0007 | g0180 | AFR | ESN | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0268 | AFR | ESN | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | ESN | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG03139 | hp2 | a0001 | c0002 | t0007 | g0229 | AFR | ESN | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0325 | AFR | ESN | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | ESN | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0240 | AFR | MSL | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG03209 | hp2 | a0001 | c0002 | t0002 | g0145 | AFR | MSL | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG03225 | hp1 | a0001 | c0002 | t0012 | g0146 | AFR | MSL | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG03225 | hp2 | a0001 | c0002 | t0002 | g0050 | AFR | MSL | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG03239 | hp1 | a0003 | c0006 | t0001 | g0318 | SAS | PJL | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0037 | SAS | PJL | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0327 | AFR | MSL | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG03453 | hp2 | a0001 | c0002 | t0013 | g0239 | AFR | MSL | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0094 | SAS | PJL | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG03492 | hp2 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG03516 | hp1 | a0001 | c0002 | t0010 | g0258 | AFR | ESN | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG03516 | hp2 | a0001 | c0002 | t0011 | g0010 | AFR | ESN | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | GWD | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG03540 | hp2 | a0001 | c0002 | t0007 | g0138 | AFR | GWD | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG03579 | hp1 | a0001 | c0002 | t0014 | g0140 | AFR | MSL | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG03579 | hp2 | a0001 | c0001 | t0019 | g0223 | AFR | MSL | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG03654 | hp2 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0304 | SAS | PJL | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG03669 | hp2 | a0001 | c0002 | t0001 | g0042 | SAS | PJL | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG03688 | hp1 | a0001 | c0002 | t0001 | g0014 | SAS | STU | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0046 | SAS | STU | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0043 | SAS | PJL | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0078 | SAS | PJL | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0322 | SAS | PJL | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0187 | SAS | BEB | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0222 | SAS | BEB | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0302 | SAS | BEB | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0133 | SAS | STU | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0190 | SAS | STU | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0321 | SAS | BEB | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0352 | SAS | BEB | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0061 | SAS | STU | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0219 | SAS | STU | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0192 | SAS | STU | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0199 | SAS | STU | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | STU | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0186 | SAS | STU | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA18522 | hp1 | a0001 | c0002 | t0003 | g0228 | AFR | YRI | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | YRI | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | CHB | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0362 | EAS | CHB | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA18906 | hp1 | a0001 | c0002 | t0005 | g0274 | AFR | YRI | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0323 | AFR | YRI | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA18947 | hp1 | a0001 | c0002 | t0001 | g0124 | EAS | JPT | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0349 | EAS | JPT | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA18948 | hp2 | a0001 | c0002 | t0001 | g0297 | EAS | JPT | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA18951 | hp2 | a0001 | c0002 | t0006 | g0047 | EAS | JPT | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA18952 | hp2 | a0001 | c0002 | t0001 | g0125 | EAS | JPT | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA18960 | hp1 | a0001 | c0002 | t0001 | g0248 | EAS | JPT | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA18967 | hp1 | a0001 | c0002 | t0001 | g0121 | EAS | JPT | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA18969 | hp2 | a0001 | c0002 | t0001 | g0128 | EAS | JPT | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0364 | EAS | JPT | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA18973 | hp2 | a0001 | c0002 | t0006 | g0028 | EAS | JPT | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA18977 | hp2 | a0001 | c0002 | t0001 | g0024 | EAS | JPT | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA18981 | hp2 | a0001 | c0002 | t0001 | g0118 | EAS | JPT | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA18985 | hp2 | a0001 | c0002 | t0001 | g0017 | EAS | JPT | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA18986 | hp1 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA18986 | hp2 | a0001 | c0002 | t0008 | g0255 | EAS | JPT | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0342 | EAS | JPT | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA18988 | hp2 | a0001 | c0002 | t0001 | g0122 | EAS | JPT | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA18989 | hp1 | a0001 | c0002 | t0004 | g0254 | EAS | JPT | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0353 | EAS | JPT | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA18998 | hp2 | a0001 | c0002 | t0001 | g0020 | EAS | JPT | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA19002 | hp2 | a0001 | c0002 | t0006 | g0038 | EAS | JPT | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA19009 | hp1 | a0001 | c0001 | t0018 | g0184 | EAS | JPT | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0344 | AFR | LWK | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0286 | AFR | LWK | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA19043 | hp1 | a0001 | c0002 | t0001 | g0330 | AFR | LWK | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0324 | AFR | LWK | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA19056 | hp2 | a0001 | c0002 | t0001 | g0123 | EAS | JPT | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0361 | EAS | JPT | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA19067 | hp2 | a0001 | c0002 | t0001 | g0012 | EAS | JPT | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA19068 | hp2 | a0001 | c0002 | t0001 | g0260 | EAS | JPT | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA19081 | hp2 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0345 | EAS | JPT | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA19083 | hp1 | a0001 | c0002 | t0008 | g0256 | EAS | JPT | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0241 | AFR | ASW | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0357 | AFR | ASW | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0039 | EUR | TSI | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA20752 | hp2 | a0001 | c0002 | t0004 | g0246 | EUR | TSI | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA20805 | hp1 | a0001 | c0001 | t0009 | g0167 | EUR | TSI | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0006 | EUR | TSI | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0308 | SAS | GIH | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA20905 | hp2 | a0001 | c0002 | t0001 | g0022 | SAS | GIH | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0339 | AFR | ACB | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | ACB | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG02486 | hp1 | a0001 | c0002 | t0003 | g0225 | AFR | ACB | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | ACB | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0232 | AFR | ACB | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG02559 | hp2 | a0001 | c0002 | t0005 | g0273 | AFR | ACB | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0358 | AFR | USA | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| HG06807 | hp2 | a0001 | c0002 | t0003 | g0141 | AFR | USA | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA18955 | hp2 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0266 | AFR | USA | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | USA | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0351 | AFR | LWK | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0340 | AFR | LWK | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0329 | REF | REF | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| homoSapiens_grch38 | hp1 | a0001 | c0002 | t0001 | g0238 | REF | REF | FAM81A_chr15_59433186_59528555 | FAM81A | chr15 | 59433186 | 59528555 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:59514297
|
G | T | 1 | a0004 | 1 | HG00323.hp2 | missense_variant | MODERATE | c.659G>T | p.Gly220Val | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 7/9 | 833/3458 | 659/1107 | 220/368 | chr15 | 59514297 | ||
| chr15:59516821
|
G | A | 1 | a0003 | 1 | HG03239.hp1 | missense_variant | MODERATE | c.963G>A | p.Met321Ile | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 8/9 | 1137/3458 | 963/1107 | 321/368 | chr15 | 59516821 | ||
| chr15:59521265
|
G | A | 1 | a0002 | 2 | HG01261.hp1 HG01516.hp2 |
missense_variant | MODERATE | c.994G>A | p.Val332Ile | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 9/9 | 1168/3458 | 994/1107 | 332/368 | chr15 | 59521265 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:59460053
|
C | T | 1 | a0001c0003 | 4 | HG02622.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
synonymous_variant | LOW | c.141C>T | p.Leu47Leu | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/9 | 315/3458 | 141/1107 | 47/368 | chr15 | 59460053 | ||
| chr15:59492294
|
C | T | 4 | a0001c0001a0002c0007a0003c0006others(1): Show | 287 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(284): Show |
synonymous_variant | LOW | c.318C>T | p.Ala106Ala | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/9 | 492/3458 | 318/1107 | 106/368 | chr15 | 59492294 | ||
| chr15:59521288
|
C | T | 2 | a0001c0003a0001c0005 | 5 | HG02622.hp1 HG02630.hp1 HG02896.hp2 others(2): Show |
synonymous_variant | LOW | c.1017C>T | p.Leu339Leu | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 9/9 | 1191/3458 | 1017/1107 | 339/368 | chr15 | 59521288 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:59438214
|
C | T | 1 | a0001c0001t0019 | 1 | HG03579.hp2 | 5_prime_UTR_variant | MODIFIER | c.-146C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/9 | 20413 | chr15 | 59438214 | |||||
| chr15:59438215
|
A | G | 1 | a0001c0001t0018 | 1 | NA19009.hp1 | 5_prime_UTR_variant | MODIFIER | c.-145A>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/9 | 20412 | chr15 | 59438215 | |||||
| chr15:59438250
|
T | C | 1 | a0001c0002t0008 | 2 | NA18986.hp2 NA19083.hp1 |
5_prime_UTR_variant | MODIFIER | c.-110T>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/9 | 20377 | chr15 | 59438250 | |||||
| chr15:59458580
|
C | T | 1 | a0001c0001t0017 | 1 | HG03017.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-47C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 2/9 | chr15 | 59458580 | ||||||
| chr15:59521671
|
A | G | 1 | a0001c0002t0005 | 6 | HG02258.hp1 HG02559.hp2 HG02723.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*293A>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 9/9 | 293 | chr15 | 59521671 | |||||
| chr15:59521922
|
A | C | 1 | a0001c0002t0007 | 3 | HG03130.hp1 HG03139.hp2 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*544A>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 9/9 | 544 | chr15 | 59521922 | |||||
| chr15:59522047
|
G | A | 1 | a0001c0001t0009 | 2 | HG01361.hp2 NA20805.hp1 |
3_prime_UTR_variant | MODIFIER | c.*669G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 9/9 | 669 | chr15 | 59522047 | |||||
| chr15:59522106
|
C | T | 1 | a0001c0001t0016 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*728C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 9/9 | 728 | chr15 | 59522106 | |||||
| chr15:59522357
|
G | A | 2 | a0001c0002t0010a0001c0002t0012 | 3 | HG03098.hp1 HG03225.hp1 HG03516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*979G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 9/9 | 979 | chr15 | 59522357 | |||||
| chr15:59522652
|
C | T | 1 | a0001c0002t0012 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1274C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 9/9 | 1274 | chr15 | 59522652 | |||||
| chr15:59522754
|
A | T | 1 | a0001c0002t0015 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1376A>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 9/9 | 1376 | chr15 | 59522754 | |||||
| chr15:59523043
|
C | T | 4 | a0001c0002t0003a0001c0002t0007a0001c0002t0014others(1): Show | 12 | HG01884.hp2 HG02451.hp2 HG02486.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1665C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 9/9 | 1665 | chr15 | 59523043 | |||||
| chr15:59523082
|
C | T | 3 | a0001c0002t0002a0001c0003t0002a0001c0005t0002 | 7 | HG02622.hp1 HG02630.hp1 HG02896.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1704C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 9/9 | 1704 | chr15 | 59523082 | |||||
| chr15:59523282
|
T | G | 5 | a0001c0002t0003a0001c0002t0007a0001c0002t0013others(2): Show | 13 | HG01884.hp2 HG02451.hp2 HG02486.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1904T>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 9/9 | 1904 | chr15 | 59523282 | |||||
| chr15:59523291
|
T | C | 9 | a0001c0002t0002a0001c0002t0004a0001c0002t0008others(6): Show | 20 | HG01109.hp1 HG01516.hp2 HG02622.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*1913T>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 9/9 | 1913 | chr15 | 59523291 | |||||
| chr15:59523380
|
C | T | 1 | a0001c0002t0011 | 2 | HG02970.hp2 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2002C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 9/9 | 2002 | chr15 | 59523380 | |||||
| chr15:59523394
|
C | T | 1 | a0001c0002t0006 | 3 | NA18951.hp2 NA18973.hp2 NA19002.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2016C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 9/9 | 2016 | chr15 | 59523394 | |||||
| chr15:59523446
|
G | A | 4 | a0001c0002t0003a0001c0002t0007a0001c0002t0013others(1): Show | 12 | HG01884.hp2 HG02451.hp2 HG02486.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2068G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 9/9 | 2068 | chr15 | 59523446 | |||||
| chr15:59523529
|
A | ATTAAAAA others(7): Show |
1 | a0001c0001t0016 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2151_*2152insTTAA others(10): Show |
FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 9/9 | 2152 | chr15 | 59523529 | |||||
| chr15:59523533
|
G | A | 1 | a0001c0001t0016 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2155G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 9/9 | 2155 | chr15 | 59523533 | |||||
| chr15:59523544
|
T | A | 1 | a0001c0001t0016 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2166T>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 9/9 | 2166 | chr15 | 59523544 | |||||
| chr15:59523545
|
T | A | 1 | a0001c0001t0016 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2167T>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 9/9 | 2167 | chr15 | 59523545 | |||||
| chr15:59523546
|
T | A | 1 | a0001c0001t0016 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2168T>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 9/9 | 2168 | chr15 | 59523546 | |||||
| chr15:59523547
|
T | A | 1 | a0001c0001t0016 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2169T>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 9/9 | 2169 | chr15 | 59523547 | |||||
| chr15:59523548
|
C | A | 1 | a0001c0001t0016 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2170C>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 9/9 | 2170 | chr15 | 59523548 | |||||
| chr15:59523550
|
C | A | 1 | a0001c0001t0016 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2172C>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 9/9 | 2172 | chr15 | 59523550 | |||||
| chr15:59523552
|
T | A | 1 | a0001c0001t0016 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2174T>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 9/9 | 2174 | chr15 | 59523552 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:59438694
|
G | A | 1 | a0001c0002t0001g0011 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-78+412G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59438694 | ||||||
| chr15:59438931
|
T | A | 177 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(174): Show | 185 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.-78+649T>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59438931 | ||||||
| chr15:59439107
|
T | C | 2 | a0001c0002t0001g0012a0001c0002t0001g0013 | 2 | NA18955.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.-78+825T>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59439107 | ||||||
| chr15:59439113
|
C | CGT | 105 | a0001c0001t0001g0261a0001c0001t0001g0262a0001c0001t0001g0263others(102): Show | 106 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.-78+843_-78+844dup others(2): Show |
FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr15 | 59439113 | |||||
| chr15:59439113
|
C | T | 1 | a0001c0001t0001g0364 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.-78+831C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59439113 | ||||||
| chr15:59439115
|
T | C | 1 | a0001c0002t0001g0014 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-78+833T>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59439115 | ||||||
| chr15:59439171
|
C | A | 1 | a0001c0002t0007g0180 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-78+889C>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59439171 | ||||||
| chr15:59439387
|
T | C | 1 | a0001c0001t0001g0181 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-78+1105T>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59439387 | ||||||
| chr15:59439408
|
T | TG | 43 | a0001c0001t0001g0144a0001c0001t0001g0147a0001c0001t0001g0148others(40): Show | 43 | HG00733.hp1 HG01074.hp1 HG01081.hp1 others(40): Show |
intron_variant | MODIFIER | c.-78+1134dupG | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr15 | 59439408 | |||||
| chr15:59439425
|
T | G | 87 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0016others(84): Show | 91 | HG00099.hp1 HG00642.hp1 HG00673.hp2 others(88): Show |
intron_variant | MODIFIER | c.-78+1143T>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59439425 | ||||||
| chr15:59439523
|
G | A | 1 | a0001c0001t0001g0182 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-78+1241G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59439523 | ||||||
| chr15:59439579
|
C | G | 17 | a0001c0001t0001g0243a0001c0001t0001g0245a0001c0001t0001g0249others(14): Show | 17 | HG01109.hp1 HG01516.hp2 HG02735.hp1 others(14): Show |
intron_variant | MODIFIER | c.-78+1297C>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59439579 | ||||||
| chr15:59439625
|
A | T | 1 | a0001c0001t0001g0242 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.-78+1343A>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59439625 | ||||||
| chr15:59439632
|
TGGGTTGG others(3): Show |
T | 1 | a0001c0001t0001g0054 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-78+1352_-78+1361d others(12): Show |
FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr15 | 59439632 | |||||
| chr15:59439645
|
C | G | 1 | a0001c0001t0001g0054 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-78+1363C>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59439645 | ||||||
| chr15:59439656
|
A | G | 1 | a0001c0002t0001g0053 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-78+1374A>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59439656 | ||||||
| chr15:59439658
|
G | C | 1 | a0001c0001t0001g0054 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-78+1376G>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59439658 | ||||||
| chr15:59439659
|
C | G | 1 | a0001c0001t0001g0054 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-78+1377C>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59439659 | ||||||
| chr15:59439660
|
T | A | 1 | a0001c0001t0001g0054 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-78+1378T>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59439660 | ||||||
| chr15:59439665
|
A | T | 43 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0016others(40): Show | 47 | HG00099.hp1 HG00642.hp1 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.-78+1383A>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59439665 | ||||||
| chr15:59439677
|
CA | C | 43 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0016others(40): Show | 47 | HG00099.hp1 HG00642.hp1 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.-78+1397delA | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr15 | 59439677 | |||||
| chr15:59439684
|
G | GGGACGAG others(49): Show |
1 | a0001c0001t0001g0054 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-78+1402_-78+1403i others(58): Show |
FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59439684 | ||||||
| chr15:59439713
|
G | A | 1 | a0001c0001t0001g0054 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-78+1431G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59439713 | ||||||
| chr15:59439758
|
T | C | 149 | a0001c0001t0001g0009a0001c0001t0001g0181a0001c0001t0001g0183others(146): Show | 151 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(148): Show |
intron_variant | MODIFIER | c.-78+1476T>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59439758 | ||||||
| chr15:59439829
|
G | C | 360 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(357): Show | 370 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(367): Show |
intron_variant | MODIFIER | c.-78+1547G>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59439829 | ||||||
| chr15:59439885
|
C | T | 4 | a0001c0001t0001g0134a0001c0001t0001g0137a0001c0002t0001g0135others(1): Show | 4 | HG02109.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-78+1603C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59439885 | ||||||
| chr15:59439897
|
A | C | 85 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0016others(82): Show | 89 | HG00099.hp1 HG00642.hp1 HG00673.hp2 others(86): Show |
intron_variant | MODIFIER | c.-78+1615A>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59439897 | ||||||
| chr15:59439903
|
C | A | 33 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(30): Show | 33 | HG00733.hp1 HG01074.hp1 HG01081.hp1 others(30): Show |
intron_variant | MODIFIER | c.-78+1621C>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59439903 | ||||||
| chr15:59439949
|
A | C | 362 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(359): Show | 372 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(369): Show |
intron_variant | MODIFIER | c.-78+1667A>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59439949 | ||||||
| chr15:59439960
|
C | T | 1 | a0001c0002t0004g0015 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-78+1678C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59439960 | ||||||
| chr15:59439992
|
T | G | 1 | a0001c0001t0001g0183 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-78+1710T>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59439992 | ||||||
| chr15:59440032
|
A | G | 77 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0016others(74): Show | 81 | HG00099.hp1 HG00642.hp1 HG00673.hp2 others(78): Show |
intron_variant | MODIFIER | c.-78+1750A>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59440032 | ||||||
| chr15:59440117
|
T | A | 76 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0016others(73): Show | 80 | HG00099.hp1 HG00642.hp1 HG00673.hp2 others(77): Show |
intron_variant | MODIFIER | c.-78+1835T>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59440117 | ||||||
| chr15:59440398
|
G | C | 6 | a0001c0001t0001g0261a0001c0001t0001g0262a0001c0001t0001g0263others(3): Show | 6 | HG00544.hp1 NA18945.hp1 NA18972.hp1 others(3): Show |
intron_variant | MODIFIER | c.-78+2116G>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59440398 | ||||||
| chr15:59440430
|
A | C | 8 | a0001c0001t0001g0230a0001c0001t0001g0231a0001c0001t0001g0232others(5): Show | 8 | HG01109.hp2 HG01243.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.-78+2148A>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59440430 | ||||||
| chr15:59440475
|
C | T | 7 | a0001c0001t0001g0173a0001c0001t0001g0174a0001c0001t0001g0175others(4): Show | 7 | HG00733.hp1 HG01081.hp1 HG01168.hp2 others(4): Show |
intron_variant | MODIFIER | c.-78+2193C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59440475 | ||||||
| chr15:59440649
|
A | G | 5 | a0001c0002t0002g0050a0001c0003t0002g0004a0001c0003t0002g0051others(2): Show | 6 | HG02622.hp1 HG02630.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.-78+2367A>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59440649 | ||||||
| chr15:59440666
|
C | T | 33 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(30): Show | 33 | HG00733.hp1 HG01074.hp1 HG01081.hp1 others(30): Show |
intron_variant | MODIFIER | c.-78+2384C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59440666 | ||||||
| chr15:59440667
|
T | C | 33 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(30): Show | 33 | HG00733.hp1 HG01074.hp1 HG01081.hp1 others(30): Show |
intron_variant | MODIFIER | c.-78+2385T>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59440667 | ||||||
| chr15:59440786
|
C | T | 1 | a0001c0001t0001g0147 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-78+2504C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59440786 | ||||||
| chr15:59440889
|
G | A | 1 | a0001c0001t0001g0055 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-78+2607G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59440889 | ||||||
| chr15:59440947
|
C | T | 17 | a0001c0001t0001g0243a0001c0001t0001g0245a0001c0001t0001g0249others(14): Show | 17 | HG01109.hp1 HG01516.hp2 HG02735.hp1 others(14): Show |
intron_variant | MODIFIER | c.-78+2665C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59440947 | ||||||
| chr15:59441005
|
C | T | 1 | a0001c0001t0001g0133 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-78+2723C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59441005 | ||||||
| chr15:59441018
|
T | C | 1 | a0001c0001t0001g0016 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-78+2736T>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59441018 | ||||||
| chr15:59441094
|
A | G | 1 | a0001c0001t0009g0132 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-78+2812A>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59441094 | ||||||
| chr15:59441351
|
T | C | 360 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(357): Show | 370 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(367): Show |
intron_variant | MODIFIER | c.-78+3069T>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59441351 | ||||||
| chr15:59441593
|
T | G | 5 | a0001c0002t0002g0050a0001c0003t0002g0004a0001c0003t0002g0051others(2): Show | 6 | HG02622.hp1 HG02630.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.-78+3311T>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59441593 | ||||||
| chr15:59441937
|
C | G | 1 | a0001c0002t0004g0015 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-78+3655C>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59441937 | ||||||
| chr15:59441994
|
G | T | 1 | a0001c0001t0001g0172 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-78+3712G>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59441994 | ||||||
| chr15:59442277
|
T | G | 17 | a0001c0001t0001g0243a0001c0001t0001g0245a0001c0001t0001g0249others(14): Show | 17 | HG01109.hp1 HG01516.hp2 HG01993.hp2 others(14): Show |
intron_variant | MODIFIER | c.-78+3995T>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59442277 | ||||||
| chr15:59442286
|
C | A | 1 | a0001c0001t0019g0223 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-78+4004C>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59442286 | ||||||
| chr15:59442297
|
A | G | 1 | a0001c0001t0001g0131 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-78+4015A>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59442297 | ||||||
| chr15:59442505
|
T | C | 1 | a0001c0001t0019g0223 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-78+4223T>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59442505 | ||||||
| chr15:59442511
|
G | A | 4 | a0001c0001t0001g0265a0001c0001t0001g0266a0001c0001t0001g0267others(1): Show | 4 | HG02145.hp2 HG02451.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-78+4229G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59442511 | ||||||
| chr15:59442618
|
CA | C | 187 | a0001c0001t0001g0009a0001c0001t0001g0046a0001c0001t0001g0129others(184): Show | 189 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(186): Show |
intron_variant | MODIFIER | c.-78+4358delA | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr15 | 59442618 | |||||
| chr15:59442636
|
A | G | 7 | a0001c0001t0001g0226a0001c0002t0001g0224a0001c0002t0003g0225others(4): Show | 7 | HG02280.hp2 HG02486.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.-78+4354A>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59442636 | ||||||
| chr15:59442684
|
C | T | 1 | a0001c0001t0001g0222 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-78+4402C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59442684 | ||||||
| chr15:59442777
|
G | C | 151 | a0001c0001t0001g0009a0001c0001t0001g0046a0001c0001t0001g0129others(148): Show | 153 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(150): Show |
intron_variant | MODIFIER | c.-78+4495G>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59442777 | ||||||
| chr15:59442966
|
G | A | 1 | a0001c0001t0018g0184 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-78+4684G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59442966 | ||||||
| chr15:59442984
|
G | A | 137 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(134): Show | 141 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(138): Show |
intron_variant | MODIFIER | c.-78+4702G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59442984 | ||||||
| chr15:59443130
|
C | T | 1 | a0001c0001t0009g0132 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-78+4848C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59443130 | ||||||
| chr15:59443146
|
A | G | 138 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(135): Show | 142 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(139): Show |
intron_variant | MODIFIER | c.-78+4864A>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59443146 | ||||||
| chr15:59443169
|
G | A | 1 | a0001c0001t0001g0057 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-78+4887G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59443169 | ||||||
| chr15:59443283
|
C | T | 6 | a0001c0002t0001g0011a0001c0002t0002g0050a0001c0003t0002g0004others(3): Show | 7 | HG01891.hp1 HG02622.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.-78+5001C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59443283 | ||||||
| chr15:59443291
|
A | G | 7 | a0001c0001t0001g0226a0001c0002t0001g0224a0001c0002t0003g0225others(4): Show | 7 | HG02280.hp2 HG02486.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.-78+5009A>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59443291 | ||||||
| chr15:59443446
|
C | G | 309 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(306): Show | 315 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(312): Show |
intron_variant | MODIFIER | c.-78+5164C>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59443446 | ||||||
| chr15:59443505
|
C | T | 1 | a0001c0001t0001g0272 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-78+5223C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59443505 | ||||||
| chr15:59443677
|
G | C | 1 | a0001c0002t0001g0224 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-78+5395G>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59443677 | ||||||
| chr15:59443706
|
C | T | 1 | a0001c0001t0001g0129 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.-78+5424C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59443706 | ||||||
| chr15:59443752
|
G | A | 1 | a0001c0001t0001g0287 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-78+5470G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59443752 | ||||||
| chr15:59443846
|
C | T | 7 | a0001c0001t0001g0226a0001c0002t0001g0224a0001c0002t0003g0225others(4): Show | 7 | HG02280.hp2 HG02486.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.-78+5564C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59443846 | ||||||
| chr15:59443896
|
C | T | 1 | a0001c0001t0001g0285 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.-78+5614C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59443896 | ||||||
| chr15:59444121
|
A | G | 155 | a0001c0001t0001g0009a0001c0001t0001g0046a0001c0001t0001g0129others(152): Show | 157 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(154): Show |
intron_variant | MODIFIER | c.-78+5839A>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59444121 | ||||||
| chr15:59444143
|
A | G | 165 | a0001c0001t0001g0009a0001c0001t0001g0046a0001c0001t0001g0129others(162): Show | 167 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(164): Show |
intron_variant | MODIFIER | c.-78+5861A>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59444143 | ||||||
| chr15:59444525
|
C | T | 146 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(143): Show | 150 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(147): Show |
intron_variant | MODIFIER | c.-78+6243C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59444525 | ||||||
| chr15:59444563
|
C | G | 161 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(158): Show | 166 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(163): Show |
intron_variant | MODIFIER | c.-78+6281C>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59444563 | ||||||
| chr15:59444720
|
G | A | 146 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(143): Show | 150 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(147): Show |
intron_variant | MODIFIER | c.-78+6438G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59444720 | ||||||
| chr15:59444729
|
C | T | 1 | a0001c0001t0001g0268 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-78+6447C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59444729 | ||||||
| chr15:59444746
|
C | T | 146 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(143): Show | 150 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(147): Show |
intron_variant | MODIFIER | c.-78+6464C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59444746 | ||||||
| chr15:59445033
|
A | G | 1 | a0001c0002t0013g0239 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-78+6751A>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59445033 | ||||||
| chr15:59445054
|
G | T | 1 | a0001c0001t0001g0144 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-78+6772G>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59445054 | ||||||
| chr15:59445058
|
A | T | 1 | a0001c0001t0001g0120 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-78+6776A>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59445058 | ||||||
| chr15:59445113
|
C | CG | 5 | a0001c0001t0001g0045a0001c0001t0001g0269a0001c0002t0001g0017others(2): Show | 5 | HG00673.hp2 HG01358.hp2 NA18967.hp1 others(2): Show |
intron_variant | MODIFIER | c.-78+6834dupG | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr15 | 59445113 | |||||
| chr15:59445157
|
C | T | 1 | a0001c0001t0001g0044 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.-78+6875C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59445157 | ||||||
| chr15:59445172
|
G | A | 2 | a0001c0001t0001g0130a0001c0001t0019g0223 | 2 | HG03579.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.-78+6890G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59445172 | ||||||
| chr15:59445194
|
C | G | 5 | a0001c0001t0001g0226a0001c0002t0001g0224a0001c0002t0003g0225others(2): Show | 5 | HG02280.hp2 HG02486.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.-78+6912C>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59445194 | ||||||
| chr15:59445307
|
G | A | 135 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(132): Show | 139 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(136): Show |
intron_variant | MODIFIER | c.-78+7025G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59445307 | ||||||
| chr15:59445399
|
C | T | 1 | a0001c0001t0001g0221 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-78+7117C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59445399 | ||||||
| chr15:59445416
|
C | T | 17 | a0001c0001t0001g0243a0001c0001t0001g0245a0001c0001t0001g0249others(14): Show | 17 | HG01109.hp1 HG01516.hp2 HG01993.hp2 others(14): Show |
intron_variant | MODIFIER | c.-78+7134C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59445416 | ||||||
| chr15:59445641
|
A | G | 17 | a0001c0001t0001g0243a0001c0001t0001g0245a0001c0001t0001g0249others(14): Show | 17 | HG01109.hp1 HG01516.hp2 HG01993.hp2 others(14): Show |
intron_variant | MODIFIER | c.-78+7359A>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59445641 | ||||||
| chr15:59445776
|
G | A | 1 | a0001c0002t0004g0015 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-78+7494G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59445776 | ||||||
| chr15:59445860
|
T | C | 1 | a0001c0001t0001g0287 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-78+7578T>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59445860 | ||||||
| chr15:59445966
|
A | T | 98 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(95): Show | 102 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.-78+7684A>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59445966 | ||||||
| chr15:59446453
|
A | G | 1 | a0001c0001t0001g0354 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.-78+8171A>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59446453 | ||||||
| chr15:59446527
|
C | T | 1 | a0001c0001t0001g0119 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-78+8245C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59446527 | ||||||
| chr15:59446671
|
C | A | 7 | a0001c0002t0001g0011a0001c0002t0002g0050a0001c0002t0002g0145others(4): Show | 8 | HG01891.hp1 HG02622.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.-78+8389C>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59446671 | ||||||
| chr15:59446900
|
T | C | 2 | a0001c0001t0001g0019a0001c0002t0001g0020 | 2 | HG02135.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.-78+8618T>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59446900 | ||||||
| chr15:59446981
|
C | G | 17 | a0001c0001t0001g0243a0001c0001t0001g0245a0001c0001t0001g0249others(14): Show | 17 | HG01109.hp1 HG01516.hp2 HG01993.hp2 others(14): Show |
intron_variant | MODIFIER | c.-78+8699C>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59446981 | ||||||
| chr15:59447121
|
C | A | 1 | a0001c0001t0001g0288 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-78+8839C>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59447121 | ||||||
| chr15:59447178
|
C | T | 9 | a0001c0001t0001g0144a0001c0001t0001g0147a0001c0002t0003g0139others(6): Show | 9 | HG01884.hp2 HG02451.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.-78+8896C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59447178 | ||||||
| chr15:59447260
|
A | G | 1 | a0001c0001t0001g0170 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-78+8978A>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59447260 | ||||||
| chr15:59447309
|
C | G | 2 | a0001c0002t0010g0257a0001c0002t0010g0258 | 2 | HG03098.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-78+9027C>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59447309 | ||||||
| chr15:59447392
|
G | A | 1 | a0001c0002t0001g0021 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-78+9110G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59447392 | ||||||
| chr15:59447417
|
A | G | 1 | a0001c0001t0001g0353 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.-78+9135A>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59447417 | ||||||
| chr15:59447630
|
A | G | 1 | a0001c0001t0001g0284 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-78+9348A>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59447630 | ||||||
| chr15:59447658
|
G | C | 17 | a0001c0001t0001g0243a0001c0001t0001g0245a0001c0001t0001g0249others(14): Show | 17 | HG01109.hp1 HG01516.hp2 HG01993.hp2 others(14): Show |
intron_variant | MODIFIER | c.-78+9376G>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59447658 | ||||||
| chr15:59447698
|
C | T | 1 | a0001c0001t0001g0172 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-78+9416C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59447698 | ||||||
| chr15:59447707
|
T | C | 1 | a0001c0001t0009g0132 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-78+9425T>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59447707 | ||||||
| chr15:59447717
|
A | G | 1 | a0001c0002t0001g0118 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.-78+9435A>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59447717 | ||||||
| chr15:59447755
|
A | G | 3 | a0001c0002t0004g0254a0001c0002t0008g0255a0001c0002t0008g0256 | 3 | NA18986.hp2 NA18989.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.-78+9473A>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59447755 | ||||||
| chr15:59447876
|
G | T | 1 | a0001c0001t0001g0171 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-78+9594G>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59447876 | ||||||
| chr15:59448020
|
G | A | 82 | a0001c0001t0001g0046a0001c0001t0001g0129a0001c0001t0001g0152others(79): Show | 83 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.-78+9738G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59448020 | ||||||
| chr15:59448170
|
C | T | 5 | a0001c0001t0001g0226a0001c0002t0001g0224a0001c0002t0003g0225others(2): Show | 5 | HG02280.hp2 HG02486.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.-78+9888C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59448170 | ||||||
| chr15:59448212
|
A | T | 2 | a0001c0001t0001g0116a0001c0001t0001g0117 | 2 | HG02129.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.-78+9930A>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59448212 | ||||||
| chr15:59448302
|
G | A | 7 | a0001c0002t0001g0011a0001c0002t0002g0050a0001c0002t0002g0145others(4): Show | 8 | HG01891.hp1 HG02622.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.-78+10020G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59448302 | ||||||
| chr15:59448350
|
C | T | 17 | a0001c0001t0001g0243a0001c0001t0001g0245a0001c0001t0001g0249others(14): Show | 17 | HG01109.hp1 HG01516.hp2 HG01993.hp2 others(14): Show |
intron_variant | MODIFIER | c.-78+10068C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59448350 | ||||||
| chr15:59448415
|
C | G | 1 | a0001c0002t0012g0146 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-78+10133C>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59448415 | ||||||
| chr15:59448459
|
G | C | 1 | a0001c0002t0012g0146 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-77-10091G>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59448459 | ||||||
| chr15:59448526
|
A | AAGATAGA others(5): Show |
16 | a0001c0001t0001g0243a0001c0001t0001g0245a0001c0001t0001g0249others(13): Show | 16 | HG01109.hp1 HG01993.hp2 HG02735.hp1 others(13): Show |
intron_variant | MODIFIER | c.-77-10021_-77-1001 others(16): Show |
FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr15 | 59448526 | |||||
| chr15:59448526
|
A | AAGATAGA others(9): Show |
1 | a0002c0004t0004g0253 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-77-10010_-77-1000 others(20): Show |
FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr15 | 59448526 | |||||
| chr15:59448541
|
G | A | 17 | a0001c0001t0001g0243a0001c0001t0001g0245a0001c0001t0001g0249others(14): Show | 17 | HG01109.hp1 HG01516.hp2 HG01993.hp2 others(14): Show |
intron_variant | MODIFIER | c.-77-10009G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59448541 | ||||||
| chr15:59448587
|
G | GT | 25 | a0001c0001t0001g0243a0001c0001t0001g0245a0001c0001t0001g0249others(22): Show | 26 | HG01192.hp2 HG01516.hp2 HG01891.hp1 others(23): Show |
intron_variant | MODIFIER | c.-77-9953dupT | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr15 | 59448587 | |||||
| chr15:59449012
|
T | C | 17 | a0001c0001t0001g0243a0001c0001t0001g0245a0001c0001t0001g0249others(14): Show | 17 | HG01109.hp1 HG01516.hp2 HG01993.hp2 others(14): Show |
intron_variant | MODIFIER | c.-77-9538T>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59449012 | ||||||
| chr15:59449176
|
T | A | 17 | a0001c0001t0001g0243a0001c0001t0001g0245a0001c0001t0001g0249others(14): Show | 17 | HG01109.hp1 HG01516.hp2 HG01993.hp2 others(14): Show |
intron_variant | MODIFIER | c.-77-9374T>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59449176 | ||||||
| chr15:59449280
|
T | C | 1 | a0001c0001t0001g0289 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-77-9270T>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59449280 | ||||||
| chr15:59449337
|
T | C | 3 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060 | 3 | HG00609.hp1 HG02074.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.-77-9213T>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59449337 | ||||||
| chr15:59449508
|
A | G | 1 | a0001c0001t0001g0362 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-77-9042A>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59449508 | ||||||
| chr15:59449548
|
A | G | 1 | a0001c0001t0001g0342 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.-77-9002A>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59449548 | ||||||
| chr15:59449557
|
G | A | 50 | a0001c0001t0001g0129a0001c0001t0001g0185a0001c0001t0001g0261others(47): Show | 50 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(47): Show |
intron_variant | MODIFIER | c.-77-8993G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59449557 | ||||||
| chr15:59449577
|
C | T | 1 | a0001c0001t0001g0283 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.-77-8973C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59449577 | ||||||
| chr15:59449597
|
C | A | 1 | a0001c0002t0001g0122 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.-77-8953C>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59449597 | ||||||
| chr15:59449597
|
C | T | 3 | a0001c0001t0001g0219a0001c0001t0001g0352a0001c0001t0017g0220 | 3 | HG03017.hp1 HG04184.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.-77-8953C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59449597 | ||||||
| chr15:59449598
|
A | G | 7 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0171others(4): Show | 7 | HG01074.hp1 HG01256.hp2 HG01258.hp2 others(4): Show |
intron_variant | MODIFIER | c.-77-8952A>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59449598 | ||||||
| chr15:59449624
|
C | T | 1 | a0001c0002t0001g0122 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.-77-8926C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59449624 | ||||||
| chr15:59449769
|
G | A | 1 | a0001c0001t0001g0342 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.-77-8781G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59449769 | ||||||
| chr15:59449781
|
CA | C | 47 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0027others(44): Show | 48 | HG00099.hp1 HG00738.hp2 HG00741.hp2 others(45): Show |
intron_variant | MODIFIER | c.-77-8739delA | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr15 | 59449781 | |||||
| chr15:59449781
|
CAA | C | 113 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0046others(110): Show | 115 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(112): Show |
intron_variant | MODIFIER | c.-77-8740_-77-8739d others(4): Show |
FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr15 | 59449781 | |||||
| chr15:59449781
|
CAAA | C | 179 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(176): Show | 184 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(181): Show |
intron_variant | MODIFIER | c.-77-8741_-77-8739d others(5): Show |
FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr15 | 59449781 | |||||
| chr15:59449781
|
CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0019g0223 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-77-8748_-77-8739d others(12): Show |
FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr15 | 59449781 | |||||
| chr15:59449783
|
A | C | 3 | a0001c0001t0001g0186a0001c0001t0001g0290a0001c0001t0001g0355 | 3 | HG02818.hp2 HG04228.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.-77-8767A>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59449783 | ||||||
| chr15:59449784
|
A | C | 109 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0046others(106): Show | 110 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(107): Show |
intron_variant | MODIFIER | c.-77-8766A>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59449784 | ||||||
| chr15:59449785
|
A | C | 179 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(176): Show | 184 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(181): Show |
intron_variant | MODIFIER | c.-77-8765A>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59449785 | ||||||
| chr15:59449786
|
A | C | 1 | a0001c0001t0001g0173 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-77-8764A>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59449786 | ||||||
| chr15:59449792
|
A | C | 1 | a0001c0001t0019g0223 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-77-8758A>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59449792 | ||||||
| chr15:59449830
|
T | A | 293 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(290): Show | 299 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(296): Show |
intron_variant | MODIFIER | c.-77-8720T>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59449830 | ||||||
| chr15:59450103
|
C | CTT | 39 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0130others(36): Show | 39 | HG00642.hp2 HG01109.hp1 HG01243.hp2 others(36): Show |
intron_variant | MODIFIER | c.-77-8432_-77-8431d others(4): Show |
FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr15 | 59450103 | |||||
| chr15:59450103
|
C | CTTT | 258 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(255): Show | 265 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(262): Show |
intron_variant | MODIFIER | c.-77-8433_-77-8431d others(5): Show |
FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr15 | 59450103 | |||||
| chr15:59450104
|
T | TTTC | 15 | a0001c0001t0001g0147a0001c0001t0001g0200a0001c0001t0001g0277others(12): Show | 15 | HG02451.hp2 HG02818.hp2 HG02895.hp2 others(12): Show |
intron_variant | MODIFIER | c.-77-8444_-77-8443i others(5): Show |
FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr15 | 59450104 | |||||
| chr15:59450170
|
A | T | 278 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(275): Show | 284 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(281): Show |
intron_variant | MODIFIER | c.-77-8380A>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59450170 | ||||||
| chr15:59450270
|
C | T | 1 | a0001c0001t0009g0132 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-77-8280C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59450270 | ||||||
| chr15:59450315
|
G | A | 1 | a0001c0001t0001g0188 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-77-8235G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59450315 | ||||||
| chr15:59450361
|
C | T | 1 | a0001c0001t0001g0322 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-77-8189C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59450361 | ||||||
| chr15:59450523
|
G | A | 7 | a0001c0002t0001g0011a0001c0002t0002g0050a0001c0002t0002g0145others(4): Show | 8 | HG01891.hp1 HG02622.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.-77-8027G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59450523 | ||||||
| chr15:59450627
|
CTT | C | 4 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0054others(1): Show | 6 | HG01081.hp2 HG01168.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.-77-7922_-77-7921d others(4): Show |
FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59450627 | ||||||
| chr15:59450722
|
C | G | 1 | a0001c0002t0012g0146 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-77-7828C>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59450722 | ||||||
| chr15:59450811
|
G | A | 300 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(297): Show | 307 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(304): Show |
intron_variant | MODIFIER | c.-77-7739G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59450811 | ||||||
| chr15:59450971
|
A | C | 1 | a0001c0001t0001g0272 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-77-7579A>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59450971 | ||||||
| chr15:59451027
|
T | C | 1 | a0001c0002t0004g0244 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-77-7523T>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59451027 | ||||||
| chr15:59451027
|
T | G | 317 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(314): Show | 324 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(321): Show |
intron_variant | MODIFIER | c.-77-7523T>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59451027 | ||||||
| chr15:59451140
|
G | T | 1 | a0001c0002t0003g0143 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-77-7410G>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59451140 | ||||||
| chr15:59451453
|
AT | A | 285 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(282): Show | 291 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(288): Show |
intron_variant | MODIFIER | c.-77-7081delT | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr15 | 59451453 | |||||
| chr15:59451453
|
ATT | A | 9 | a0001c0001t0001g0062a0001c0001t0001g0081a0001c0001t0001g0154others(6): Show | 9 | HG02486.hp1 HG02523.hp2 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.-77-7082_-77-7081d others(4): Show |
FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr15 | 59451453 | |||||
| chr15:59451539
|
G | A | 1 | a0001c0001t0001g0219 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-77-7011G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59451539 | ||||||
| chr15:59451577
|
C | T | 1 | a0001c0001t0001g0016 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-77-6973C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59451577 | ||||||
| chr15:59451670
|
G | C | 318 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(315): Show | 325 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(322): Show |
intron_variant | MODIFIER | c.-77-6880G>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59451670 | ||||||
| chr15:59451777
|
C | T | 1 | a0001c0001t0001g0199 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-77-6773C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59451777 | ||||||
| chr15:59451805
|
AC | A | 91 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(88): Show | 95 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.-77-6743delC | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr15 | 59451805 | |||||
| chr15:59451851
|
A | G | 10 | a0001c0001t0001g0144a0001c0001t0001g0147a0001c0002t0003g0139others(7): Show | 10 | HG01884.hp2 HG02451.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.-77-6699A>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59451851 | ||||||
| chr15:59452051
|
G | A | 1 | a0001c0002t0012g0146 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-77-6499G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59452051 | ||||||
| chr15:59452095
|
G | A | 363 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(360): Show | 373 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(370): Show |
intron_variant | MODIFIER | c.-77-6455G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59452095 | ||||||
| chr15:59452549
|
A | T | 1 | a0001c0001t0009g0132 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-77-6001A>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59452549 | ||||||
| chr15:59452784
|
C | T | 1 | a0001c0001t0001g0076 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.-77-5766C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59452784 | ||||||
| chr15:59452999
|
G | A | 1 | a0001c0001t0001g0362 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-77-5551G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59452999 | ||||||
| chr15:59453147
|
C | T | 7 | a0001c0002t0001g0011a0001c0002t0002g0050a0001c0002t0002g0145others(4): Show | 8 | HG01891.hp1 HG02622.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.-77-5403C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59453147 | ||||||
| chr15:59453269
|
C | T | 17 | a0001c0001t0001g0243a0001c0001t0001g0245a0001c0001t0001g0249others(14): Show | 17 | HG01109.hp1 HG01516.hp2 HG01993.hp2 others(14): Show |
intron_variant | MODIFIER | c.-77-5281C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59453269 | ||||||
| chr15:59453280
|
T | C | 294 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(291): Show | 300 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(297): Show |
intron_variant | MODIFIER | c.-77-5270T>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59453280 | ||||||
| chr15:59453409
|
A | G | 3 | a0001c0002t0004g0254a0001c0002t0008g0255a0001c0002t0008g0256 | 3 | NA18986.hp2 NA18989.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.-77-5141A>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59453409 | ||||||
| chr15:59453479
|
C | T | 2 | a0001c0001t0001g0286a0001c0001t0001g0363 | 2 | HG02965.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-77-5071C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59453479 | ||||||
| chr15:59453523
|
C | A | 315 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(312): Show | 322 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(319): Show |
intron_variant | MODIFIER | c.-77-5027C>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59453523 | ||||||
| chr15:59453541
|
T | C | 2 | a0001c0002t0010g0257a0001c0002t0010g0258 | 2 | HG03098.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-77-5009T>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59453541 | ||||||
| chr15:59453543
|
G | C | 301 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(298): Show | 308 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(305): Show |
intron_variant | MODIFIER | c.-77-5007G>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59453543 | ||||||
| chr15:59453558
|
C | G | 1 | a0001c0001t0001g0025 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-77-4992C>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59453558 | ||||||
| chr15:59453695
|
G | C | 31 | a0001c0001t0001g0077a0001c0001t0001g0148a0001c0001t0001g0149others(28): Show | 31 | HG00733.hp1 HG01074.hp1 HG01081.hp1 others(28): Show |
intron_variant | MODIFIER | c.-77-4855G>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59453695 | ||||||
| chr15:59453702
|
G | A | 1 | a0001c0001t0001g0116 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-77-4848G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59453702 | ||||||
| chr15:59453786
|
G | A | 1 | a0001c0001t0001g0362 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-77-4764G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59453786 | ||||||
| chr15:59453816
|
G | A | 294 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(291): Show | 300 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(297): Show |
intron_variant | MODIFIER | c.-77-4734G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59453816 | ||||||
| chr15:59453833
|
A | C | 2 | a0001c0001t0001g0218a0001c0001t0001g0259 | 2 | NA19081.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.-77-4717A>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59453833 | ||||||
| chr15:59453939
|
A | G | 1 | a0001c0001t0001g0144 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-77-4611A>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59453939 | ||||||
| chr15:59453972
|
G | A | 1 | a0001c0001t0001g0308 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-77-4578G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59453972 | ||||||
| chr15:59454001
|
C | T | 2 | a0001c0002t0001g0135a0001c0002t0001g0136 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-77-4549C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59454001 | ||||||
| chr15:59454009
|
C | G | 2 | a0001c0002t0010g0257a0001c0002t0010g0258 | 2 | HG03098.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-77-4541C>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59454009 | ||||||
| chr15:59454052
|
G | C | 6 | a0001c0002t0002g0050a0001c0002t0002g0145a0001c0003t0002g0004others(3): Show | 7 | HG02622.hp1 HG02630.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.-77-4498G>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59454052 | ||||||
| chr15:59454245
|
G | A | 1 | a0004c0008t0001g0309 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-77-4305G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59454245 | ||||||
| chr15:59454287
|
T | G | 1 | a0002c0007t0001g0177 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-77-4263T>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59454287 | ||||||
| chr15:59454358
|
T | C | 1 | a0001c0002t0001g0026 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-77-4192T>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59454358 | ||||||
| chr15:59454385
|
C | G | 1 | a0001c0001t0001g0025 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-77-4165C>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59454385 | ||||||
| chr15:59454591
|
T | C | 1 | a0001c0001t0001g0165 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-77-3959T>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59454591 | ||||||
| chr15:59454689
|
A | G | 1 | a0001c0001t0001g0305 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-77-3861A>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59454689 | ||||||
| chr15:59454801
|
A | AT | 7 | a0001c0002t0001g0011a0001c0002t0002g0050a0001c0002t0002g0145others(4): Show | 8 | HG01891.hp1 HG02622.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.-77-3740dupT | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr15 | 59454801 | |||||
| chr15:59454987
|
G | A | 1 | a0001c0002t0001g0330 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-77-3563G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59454987 | ||||||
| chr15:59455002
|
C | G | 1 | a0001c0001t0001g0025 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-77-3548C>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59455002 | ||||||
| chr15:59455065
|
CT | C | 10 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0355others(7): Show | 10 | HG02486.hp1 HG02818.hp2 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.-77-3469delT | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr15 | 59455065 | |||||
| chr15:59455111
|
G | T | 9 | a0001c0001t0001g0147a0001c0002t0003g0139a0001c0002t0003g0141others(6): Show | 9 | HG01884.hp2 HG02451.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.-77-3439G>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59455111 | ||||||
| chr15:59455326
|
G | A | 1 | a0001c0002t0001g0012 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.-77-3224G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59455326 | ||||||
| chr15:59455341
|
CA | C | 15 | a0001c0001t0001g0243a0001c0001t0001g0245a0001c0001t0001g0249others(12): Show | 15 | HG01109.hp1 HG01516.hp2 HG01993.hp2 others(12): Show |
intron_variant | MODIFIER | c.-77-3205delA | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr15 | 59455341 | |||||
| chr15:59455421
|
A | G | 1 | a0001c0002t0001g0042 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-77-3129A>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59455421 | ||||||
| chr15:59455429
|
A | T | 2 | a0001c0001t0001g0286a0001c0001t0001g0363 | 2 | HG02965.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-77-3121A>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59455429 | ||||||
| chr15:59455507
|
C | T | 17 | a0001c0001t0001g0243a0001c0001t0001g0245a0001c0001t0001g0249others(14): Show | 17 | HG01109.hp1 HG01516.hp2 HG01993.hp2 others(14): Show |
intron_variant | MODIFIER | c.-77-3043C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59455507 | ||||||
| chr15:59455567
|
G | A | 1 | a0001c0001t0019g0223 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-77-2983G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59455567 | ||||||
| chr15:59455605
|
A | T | 1 | a0001c0001t0001g0144 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-77-2945A>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59455605 | ||||||
| chr15:59455799
|
G | T | 1 | a0001c0002t0007g0138 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-77-2751G>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59455799 | ||||||
| chr15:59455982
|
T | A | 1 | a0001c0001t0001g0189 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-77-2568T>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59455982 | ||||||
| chr15:59456002
|
A | G | 3 | a0001c0002t0003g0225a0001c0002t0003g0228a0001c0002t0015g0227 | 3 | HG02486.hp1 HG02922.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-77-2548A>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59456002 | ||||||
| chr15:59456288
|
G | A | 2 | a0001c0001t0001g0272a0001c0001t0001g0310 | 2 | NA18961.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.-77-2262G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59456288 | ||||||
| chr15:59456289
|
G | A | 295 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(292): Show | 301 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(298): Show |
intron_variant | MODIFIER | c.-77-2261G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59456289 | ||||||
| chr15:59456365
|
A | G | 1 | a0001c0001t0001g0111 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-77-2185A>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59456365 | ||||||
| chr15:59456464
|
C | T | 295 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(292): Show | 301 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(298): Show |
intron_variant | MODIFIER | c.-77-2086C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59456464 | ||||||
| chr15:59456537
|
A | G | 1 | a0001c0001t0001g0075 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-77-2013A>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59456537 | ||||||
| chr15:59456643
|
A | G | 7 | a0001c0002t0001g0011a0001c0002t0002g0050a0001c0002t0002g0145others(4): Show | 8 | HG01891.hp1 HG02622.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.-77-1907A>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59456643 | ||||||
| chr15:59456835
|
A | C | 297 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(294): Show | 303 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(300): Show |
intron_variant | MODIFIER | c.-77-1715A>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59456835 | ||||||
| chr15:59457218
|
T | C | 312 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(309): Show | 318 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(315): Show |
intron_variant | MODIFIER | c.-77-1332T>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59457218 | ||||||
| chr15:59457304
|
C | T | 295 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(292): Show | 301 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(298): Show |
intron_variant | MODIFIER | c.-77-1246C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59457304 | ||||||
| chr15:59457363
|
G | A | 12 | a0001c0001t0001g0265a0001c0001t0001g0266a0001c0001t0001g0267others(9): Show | 12 | HG01069.hp2 HG01071.hp1 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.-77-1187G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59457363 | ||||||
| chr15:59457506
|
C | A | 1 | a0001c0002t0004g0015 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-77-1044C>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59457506 | ||||||
| chr15:59457838
|
A | G | 295 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(292): Show | 301 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(298): Show |
intron_variant | MODIFIER | c.-77-712A>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59457838 | ||||||
| chr15:59457943
|
C | T | 1 | a0001c0001t0001g0202 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.-77-607C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59457943 | ||||||
| chr15:59458106
|
C | T | 1 | a0001c0002t0003g0142 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-77-444C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59458106 | ||||||
| chr15:59458239
|
G | A | 2 | a0001c0001t0001g0286a0001c0001t0001g0363 | 2 | HG02965.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-77-311G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59458239 | ||||||
| chr15:59458294
|
G | A | 9 | a0001c0001t0001g0147a0001c0002t0003g0139a0001c0002t0003g0141others(6): Show | 9 | HG01884.hp2 HG02451.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.-77-256G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59458294 | ||||||
| chr15:59458388
|
CAT | C | 3 | a0001c0002t0003g0225a0001c0002t0003g0228a0001c0002t0015g0227 | 3 | HG02486.hp1 HG02922.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-77-159_-77-158del others(2): Show |
FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr15 | 59458388 | |||||
| chr15:59458407
|
G | A | 295 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(292): Show | 301 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(298): Show |
intron_variant | MODIFIER | c.-77-143G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59458407 | ||||||
| chr15:59458437
|
C | T | 1 | a0001c0001t0001g0304 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-77-113C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 1/8 | chr15 | 59458437 | ||||||
| chr15:59458731
|
G | A | 290 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(287): Show | 296 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(293): Show |
intron_variant | MODIFIER | c.20+85G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 2/8 | chr15 | 59458731 | ||||||
| chr15:59458761
|
A | G | 292 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(289): Show | 298 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(295): Show |
intron_variant | MODIFIER | c.20+115A>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 2/8 | chr15 | 59458761 | ||||||
| chr15:59459103
|
C | T | 3 | a0001c0002t0003g0225a0001c0002t0003g0228a0001c0002t0015g0227 | 3 | HG02486.hp1 HG02922.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.20+457C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 2/8 | chr15 | 59459103 | ||||||
| chr15:59459239
|
G | A | 295 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(292): Show | 301 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(298): Show |
intron_variant | MODIFIER | c.20+593G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 2/8 | chr15 | 59459239 | ||||||
| chr15:59459243
|
T | C | 1 | a0001c0001t0001g0349 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.20+597T>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 2/8 | chr15 | 59459243 | ||||||
| chr15:59459267
|
T | G | 1 | a0001c0002t0006g0028 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.20+621T>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 2/8 | chr15 | 59459267 | ||||||
| chr15:59459396
|
C | G | 1 | a0001c0001t0001g0303 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.21-537C>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 2/8 | chr15 | 59459396 | ||||||
| chr15:59459447
|
C | T | 15 | a0001c0001t0001g0243a0001c0001t0001g0245a0001c0001t0001g0249others(12): Show | 15 | HG01109.hp1 HG01516.hp2 HG01993.hp2 others(12): Show |
intron_variant | MODIFIER | c.21-486C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 2/8 | chr15 | 59459447 | ||||||
| chr15:59459641
|
T | C | 1 | a0001c0001t0001g0144 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.21-292T>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 2/8 | chr15 | 59459641 | ||||||
| chr15:59459673
|
C | T | 1 | a0001c0002t0005g0276 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.21-260C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 2/8 | chr15 | 59459673 | ||||||
| chr15:59459684
|
A | G | 1 | a0001c0001t0001g0039 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.21-249A>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 2/8 | chr15 | 59459684 | ||||||
| chr15:59459854
|
G | A | 319 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(316): Show | 326 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(323): Show |
intron_variant | MODIFIER | c.21-79G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 2/8 | chr15 | 59459854 | ||||||
| chr15:59460408
|
T | C | 1 | a0001c0001t0001g0082 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.294+202T>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59460408 | ||||||
| chr15:59460834
|
C | T | 1 | a0001c0002t0004g0015 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.294+628C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59460834 | ||||||
| chr15:59460835
|
G | A | 1 | a0001c0001t0001g0111 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.294+629G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59460835 | ||||||
| chr15:59461195
|
C | G | 7 | a0001c0002t0001g0011a0001c0002t0002g0050a0001c0002t0002g0145others(4): Show | 8 | HG01891.hp1 HG02622.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.294+989C>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59461195 | ||||||
| chr15:59461211
|
C | A | 3 | a0001c0002t0005g0274a0001c0002t0005g0275a0001c0002t0005g0276 | 3 | HG02723.hp1 HG02886.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.294+1005C>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59461211 | ||||||
| chr15:59461267
|
G | A | 1 | a0002c0004t0004g0253 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.294+1061G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59461267 | ||||||
| chr15:59461350
|
A | C | 1 | a0001c0001t0001g0152 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.294+1144A>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59461350 | ||||||
| chr15:59461403
|
G | A | 1 | a0001c0002t0013g0239 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.294+1197G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59461403 | ||||||
| chr15:59461437
|
A | G | 7 | a0001c0002t0001g0011a0001c0002t0002g0050a0001c0002t0002g0145others(4): Show | 8 | HG01891.hp1 HG02622.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.294+1231A>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59461437 | ||||||
| chr15:59461448
|
G | T | 3 | a0001c0001t0001g0240a0001c0001t0001g0241a0001c0001t0001g0344 | 3 | HG03209.hp1 NA19030.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.294+1242G>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59461448 | ||||||
| chr15:59461512
|
C | T | 3 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0110 | 3 | NA18983.hp2 NA19007.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.294+1306C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59461512 | ||||||
| chr15:59461887
|
T | C | 111 | a0001c0001t0001g0046a0001c0001t0001g0129a0001c0001t0001g0148others(108): Show | 112 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.294+1681T>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59461887 | ||||||
| chr15:59461931
|
C | T | 2 | a0001c0001t0001g0286a0001c0001t0001g0363 | 2 | HG02965.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.294+1725C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59461931 | ||||||
| chr15:59461969
|
C | T | 2 | a0001c0002t0001g0224a0001c0002t0001g0330 | 2 | HG02809.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.294+1763C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59461969 | ||||||
| chr15:59462064
|
G | A | 42 | a0001c0001t0001g0009a0001c0001t0001g0154a0001c0001t0001g0178others(39): Show | 43 | HG00558.hp2 HG00733.hp1 HG00738.hp1 others(40): Show |
intron_variant | MODIFIER | c.294+1858G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59462064 | ||||||
| chr15:59462196
|
G | C | 293 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(290): Show | 299 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(296): Show |
intron_variant | MODIFIER | c.294+1990G>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59462196 | ||||||
| chr15:59462202
|
C | CA | 31 | a0001c0001t0001g0063a0001c0001t0001g0083a0001c0001t0001g0231others(28): Show | 31 | HG01109.hp1 HG01243.hp2 HG01516.hp2 others(28): Show |
intron_variant | MODIFIER | c.294+2014dupA | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr15 | 59462202 | |||||
| chr15:59462220
|
A | C | 2 | a0001c0001t0001g0327a0001c0002t0003g0271 | 2 | HG02896.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.294+2014A>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59462220 | ||||||
| chr15:59462395
|
A | T | 4 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0080others(1): Show | 4 | NA18959.hp2 NA18983.hp2 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.294+2189A>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59462395 | ||||||
| chr15:59462404
|
G | A | 1 | a0001c0002t0013g0239 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.294+2198G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59462404 | ||||||
| chr15:59462425
|
T | C | 1 | a0001c0002t0001g0026 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.294+2219T>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59462425 | ||||||
| chr15:59462630
|
A | G | 3 | a0001c0002t0003g0225a0001c0002t0003g0228a0001c0002t0015g0227 | 3 | HG02486.hp1 HG02922.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.294+2424A>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59462630 | ||||||
| chr15:59462632
|
G | C | 293 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(290): Show | 299 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(296): Show |
intron_variant | MODIFIER | c.294+2426G>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59462632 | ||||||
| chr15:59462868
|
C | T | 293 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(290): Show | 299 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(296): Show |
intron_variant | MODIFIER | c.294+2662C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59462868 | ||||||
| chr15:59462908
|
A | G | 1 | a0001c0001t0001g0214 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.294+2702A>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59462908 | ||||||
| chr15:59463164
|
C | T | 1 | a0001c0001t0001g0217 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.294+2958C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59463164 | ||||||
| chr15:59463228
|
C | T | 1 | a0001c0001t0001g0165 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.294+3022C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59463228 | ||||||
| chr15:59463250
|
C | T | 3 | a0001c0001t0001g0151a0001c0001t0001g0162a0001c0001t0001g0170 | 3 | NA18960.hp2 NA19003.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.294+3044C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59463250 | ||||||
| chr15:59463300
|
G | C | 1 | a0001c0001t0001g0084 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.294+3094G>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59463300 | ||||||
| chr15:59463516
|
C | A | 293 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(290): Show | 299 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(296): Show |
intron_variant | MODIFIER | c.294+3310C>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59463516 | ||||||
| chr15:59463583
|
C | T | 3 | a0001c0002t0004g0254a0001c0002t0008g0255a0001c0002t0008g0256 | 3 | NA18986.hp2 NA18989.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.294+3377C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59463583 | ||||||
| chr15:59463690
|
C | CAAT | 9 | a0001c0001t0001g0243a0001c0001t0001g0245a0001c0001t0001g0249others(6): Show | 9 | HG02965.hp1 NA18952.hp1 NA18957.hp2 others(6): Show |
intron_variant | MODIFIER | c.294+3502_294+3504d others(5): Show |
FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr15 | 59463690 | |||||
| chr15:59463755
|
AT | A | 295 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(292): Show | 301 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(298): Show |
intron_variant | MODIFIER | c.294+3551delT | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr15 | 59463755 | |||||
| chr15:59463787
|
T | G | 5 | a0001c0001t0001g0144a0001c0002t0003g0225a0001c0002t0003g0228others(2): Show | 5 | HG02486.hp1 HG02647.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.294+3581T>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59463787 | ||||||
| chr15:59464191
|
C | T | 3 | a0001c0002t0003g0225a0001c0002t0003g0228a0001c0002t0015g0227 | 3 | HG02486.hp1 HG02922.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.294+3985C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59464191 | ||||||
| chr15:59464463
|
T | C | 295 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(292): Show | 301 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(298): Show |
intron_variant | MODIFIER | c.294+4257T>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59464463 | ||||||
| chr15:59464579
|
C | A | 1 | a0001c0001t0001g0291 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.294+4373C>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59464579 | ||||||
| chr15:59464762
|
A | C | 2 | a0001c0001t0001g0183a0001c0001t0001g0349 | 2 | NA18948.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.294+4556A>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59464762 | ||||||
| chr15:59464943
|
T | C | 1 | a0001c0001t0001g0027 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.294+4737T>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59464943 | ||||||
| chr15:59465006
|
G | A | 3 | a0001c0001t0001g0187a0001c0001t0001g0190a0001c0001t0001g0199 | 3 | HG03834.hp1 HG04115.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.294+4800G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59465006 | ||||||
| chr15:59465128
|
C | T | 139 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(136): Show | 143 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(140): Show |
intron_variant | MODIFIER | c.294+4922C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59465128 | ||||||
| chr15:59465144
|
G | A | 2 | a0001c0001t0001g0114a0001c0001t0001g0115 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.294+4938G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59465144 | ||||||
| chr15:59465305
|
C | T | 1 | a0001c0001t0001g0134 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.294+5099C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59465305 | ||||||
| chr15:59465311
|
T | C | 115 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(112): Show | 119 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(116): Show |
intron_variant | MODIFIER | c.294+5105T>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59465311 | ||||||
| chr15:59465334
|
G | A | 3 | a0001c0001t0001g0172a0001c0001t0001g0327a0001c0002t0003g0271 | 3 | HG01192.hp1 HG02896.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.294+5128G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59465334 | ||||||
| chr15:59465340
|
T | C | 1 | a0001c0002t0005g0236 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.294+5134T>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59465340 | ||||||
| chr15:59465355
|
C | G | 294 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(291): Show | 300 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(297): Show |
intron_variant | MODIFIER | c.294+5149C>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59465355 | ||||||
| chr15:59465392
|
C | T | 1 | a0001c0001t0001g0326 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.294+5186C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59465392 | ||||||
| chr15:59465622
|
G | A | 1 | a0001c0001t0001g0055 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.294+5416G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59465622 | ||||||
| chr15:59465638
|
T | C | 7 | a0001c0002t0001g0011a0001c0002t0002g0050a0001c0002t0002g0145others(4): Show | 8 | HG01891.hp1 HG02622.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.294+5432T>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59465638 | ||||||
| chr15:59465665
|
A | T | 1 | a0001c0001t0001g0329 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.294+5459A>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59465665 | ||||||
| chr15:59465759
|
A | G | 1 | a0001c0001t0001g0343 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.294+5553A>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59465759 | ||||||
| chr15:59465778
|
G | T | 1 | a0001c0001t0001g0284 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.294+5572G>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59465778 | ||||||
| chr15:59465853
|
G | A | 3 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0356 | 3 | HG02723.hp2 HG02886.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.294+5647G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59465853 | ||||||
| chr15:59466151
|
T | C | 1 | a0001c0001t0016g0166 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.294+5945T>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59466151 | ||||||
| chr15:59466202
|
A | G | 4 | a0001c0002t0005g0273a0001c0002t0005g0274a0001c0002t0005g0275others(1): Show | 4 | HG02559.hp2 HG02723.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.294+5996A>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59466202 | ||||||
| chr15:59466232
|
T | G | 1 | a0001c0002t0001g0053 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.294+6026T>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59466232 | ||||||
| chr15:59466246
|
G | A | 1 | a0001c0002t0001g0011 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.294+6040G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59466246 | ||||||
| chr15:59466276
|
G | T | 1 | a0001c0002t0001g0024 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.294+6070G>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59466276 | ||||||
| chr15:59466426
|
C | T | 295 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(292): Show | 301 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(298): Show |
intron_variant | MODIFIER | c.294+6220C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59466426 | ||||||
| chr15:59466446
|
G | A | 1 | a0001c0002t0013g0239 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.294+6240G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59466446 | ||||||
| chr15:59466478
|
G | GCTGCATA others(35): Show |
2 | a0001c0001t0001g0286a0001c0001t0001g0363 | 2 | HG02965.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.294+6272_294+6273i others(44): Show |
FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59466478 | ||||||
| chr15:59466481
|
T | C | 2 | a0001c0001t0001g0286a0001c0001t0001g0363 | 2 | HG02965.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.294+6275T>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59466481 | ||||||
| chr15:59466482
|
C | A | 2 | a0001c0001t0001g0286a0001c0001t0001g0363 | 2 | HG02965.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.294+6276C>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59466482 | ||||||
| chr15:59466485
|
T | A | 2 | a0001c0001t0001g0286a0001c0001t0001g0363 | 2 | HG02965.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.294+6279T>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59466485 | ||||||
| chr15:59466486
|
T | C | 2 | a0001c0001t0001g0286a0001c0001t0001g0363 | 2 | HG02965.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.294+6280T>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59466486 | ||||||
| chr15:59466499
|
G | C | 1 | a0001c0001t0001g0064 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.294+6293G>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59466499 | ||||||
| chr15:59466513
|
T | C | 2 | a0001c0001t0001g0085a0001c0001t0001g0086 | 2 | NA18943.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.294+6307T>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59466513 | ||||||
| chr15:59466518
|
C | G | 7 | a0001c0002t0001g0011a0001c0002t0002g0050a0001c0002t0002g0145others(4): Show | 8 | HG01891.hp1 HG02622.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.294+6312C>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59466518 | ||||||
| chr15:59466551
|
T | C | 1 | a0001c0001t0009g0167 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.294+6345T>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59466551 | ||||||
| chr15:59466673
|
G | A | 99 | a0001c0001t0001g0046a0001c0001t0001g0129a0001c0001t0001g0148others(96): Show | 100 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.294+6467G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59466673 | ||||||
| chr15:59466763
|
A | C | 1 | a0001c0001t0001g0264 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.294+6557A>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59466763 | ||||||
| chr15:59466788
|
A | G | 3 | a0001c0001t0001g0302a0001c0001t0001g0321a0001c0001t0001g0352 | 3 | HG03942.hp2 HG04184.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.294+6582A>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59466788 | ||||||
| chr15:59466982
|
G | GT | 3 | a0001c0002t0003g0225a0001c0002t0003g0228a0001c0002t0015g0227 | 3 | HG02486.hp1 HG02922.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.294+6781dupT | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr15 | 59466982 | |||||
| chr15:59467028
|
A | G | 4 | a0001c0001t0001g0261a0001c0001t0001g0263a0001c0001t0001g0264others(1): Show | 4 | NA18945.hp1 NA19060.hp2 NA19068.hp2 others(1): Show |
intron_variant | MODIFIER | c.294+6822A>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59467028 | ||||||
| chr15:59467068
|
G | A | 1 | a0001c0002t0012g0146 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.294+6862G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59467068 | ||||||
| chr15:59467118
|
G | T | 3 | a0001c0002t0006g0028a0001c0002t0006g0038a0001c0002t0006g0047 | 3 | NA18951.hp2 NA18973.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.294+6912G>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59467118 | ||||||
| chr15:59467397
|
T | C | 192 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(189): Show | 197 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(194): Show |
intron_variant | MODIFIER | c.294+7191T>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59467397 | ||||||
| chr15:59467468
|
C | G | 7 | a0001c0001t0001g0231a0001c0001t0001g0232a0001c0001t0001g0233others(4): Show | 7 | HG01243.hp2 HG02145.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.294+7262C>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59467468 | ||||||
| chr15:59467638
|
A | G | 15 | a0001c0001t0001g0243a0001c0001t0001g0245a0001c0001t0001g0249others(12): Show | 15 | HG01109.hp1 HG01516.hp2 HG01993.hp2 others(12): Show |
intron_variant | MODIFIER | c.294+7432A>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59467638 | ||||||
| chr15:59467721
|
C | T | 190 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(187): Show | 195 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(192): Show |
intron_variant | MODIFIER | c.294+7515C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59467721 | ||||||
| chr15:59467854
|
A | G | 4 | a0001c0003t0002g0004a0001c0003t0002g0051a0001c0003t0002g0052others(1): Show | 5 | HG02622.hp1 HG02630.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.294+7648A>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59467854 | ||||||
| chr15:59467969
|
T | C | 15 | a0001c0001t0001g0243a0001c0001t0001g0245a0001c0001t0001g0249others(12): Show | 15 | HG01109.hp1 HG01516.hp2 HG01993.hp2 others(12): Show |
intron_variant | MODIFIER | c.294+7763T>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59467969 | ||||||
| chr15:59468059
|
C | T | 3 | a0001c0002t0003g0225a0001c0002t0003g0228a0001c0002t0015g0227 | 3 | HG02486.hp1 HG02922.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.294+7853C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59468059 | ||||||
| chr15:59468080
|
G | A | 27 | a0001c0001t0001g0129a0001c0001t0001g0148a0001c0001t0001g0185others(24): Show | 27 | HG00423.hp2 HG00438.hp1 HG00609.hp2 others(24): Show |
intron_variant | MODIFIER | c.294+7874G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59468080 | ||||||
| chr15:59468390
|
G | A | 3 | a0001c0001t0001g0172a0001c0001t0001g0327a0001c0002t0003g0271 | 3 | HG01192.hp1 HG02896.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.294+8184G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59468390 | ||||||
| chr15:59468416
|
T | C | 1 | a0001c0001t0001g0336 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.294+8210T>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59468416 | ||||||
| chr15:59468617
|
T | C | 1 | a0001c0001t0001g0111 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.294+8411T>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59468617 | ||||||
| chr15:59468647
|
T | TA | 107 | a0001c0001t0001g0046a0001c0001t0001g0129a0001c0001t0001g0148others(104): Show | 108 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.294+8452dupA | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr15 | 59468647 | |||||
| chr15:59468659
|
C | A | 103 | a0001c0001t0001g0046a0001c0001t0001g0129a0001c0001t0001g0148others(100): Show | 104 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.294+8453C>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59468659 | ||||||
| chr15:59468662
|
A | T | 7 | a0001c0001t0001g0272a0001c0001t0001g0299a0001c0001t0001g0300others(4): Show | 7 | HG00609.hp2 NA18943.hp1 NA18961.hp1 others(4): Show |
intron_variant | MODIFIER | c.294+8456A>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59468662 | ||||||
| chr15:59468927
|
T | C | 1 | a0001c0001t0001g0087 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.294+8721T>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59468927 | ||||||
| chr15:59469163
|
G | C | 1 | a0001c0001t0001g0219 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.294+8957G>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59469163 | ||||||
| chr15:59469262
|
C | T | 3 | a0001c0002t0003g0225a0001c0002t0003g0228a0001c0002t0015g0227 | 3 | HG02486.hp1 HG02922.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.294+9056C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59469262 | ||||||
| chr15:59469407
|
A | G | 15 | a0001c0001t0001g0243a0001c0001t0001g0245a0001c0001t0001g0249others(12): Show | 15 | HG01109.hp1 HG01516.hp2 HG01993.hp2 others(12): Show |
intron_variant | MODIFIER | c.294+9201A>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59469407 | ||||||
| chr15:59469486
|
A | G | 15 | a0001c0001t0001g0243a0001c0001t0001g0245a0001c0001t0001g0249others(12): Show | 15 | HG01109.hp1 HG01516.hp2 HG01993.hp2 others(12): Show |
intron_variant | MODIFIER | c.294+9280A>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59469486 | ||||||
| chr15:59469529
|
C | G | 3 | a0001c0002t0003g0225a0001c0002t0003g0228a0001c0002t0015g0227 | 3 | HG02486.hp1 HG02922.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.294+9323C>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59469529 | ||||||
| chr15:59469538
|
CT | C | 99 | a0001c0001t0001g0046a0001c0001t0001g0129a0001c0001t0001g0148others(96): Show | 100 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.294+9345delT | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr15 | 59469538 | |||||
| chr15:59469628
|
C | T | 4 | a0001c0001t0001g0134a0001c0001t0001g0137a0001c0002t0001g0135others(1): Show | 4 | HG02109.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.294+9422C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59469628 | ||||||
| chr15:59469632
|
T | C | 1 | a0001c0001t0009g0167 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.294+9426T>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59469632 | ||||||
| chr15:59469650
|
G | A | 1 | a0001c0001t0001g0311 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.294+9444G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59469650 | ||||||
| chr15:59469678
|
G | C | 1 | a0001c0001t0001g0302 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.294+9472G>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59469678 | ||||||
| chr15:59469705
|
G | A | 12 | a0001c0001t0001g0265a0001c0001t0001g0266a0001c0001t0001g0267others(9): Show | 12 | HG01069.hp2 HG01071.hp1 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.294+9499G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59469705 | ||||||
| chr15:59469908
|
C | G | 1 | a0001c0001t0001g0217 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.294+9702C>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59469908 | ||||||
| chr15:59470015
|
T | C | 7 | a0001c0001t0001g0231a0001c0001t0001g0232a0001c0001t0001g0233others(4): Show | 7 | HG01243.hp2 HG02145.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.294+9809T>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59470015 | ||||||
| chr15:59470158
|
A | G | 7 | a0001c0001t0001g0277a0001c0001t0001g0278a0001c0001t0001g0281others(4): Show | 7 | NA18939.hp1 NA18966.hp1 NA18970.hp1 others(4): Show |
intron_variant | MODIFIER | c.294+9952A>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59470158 | ||||||
| chr15:59470230
|
T | C | 1 | a0001c0001t0001g0055 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.294+10024T>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59470230 | ||||||
| chr15:59470327
|
C | T | 41 | a0001c0001t0001g0009a0001c0001t0001g0154a0001c0001t0001g0178others(38): Show | 42 | HG00558.hp2 HG00733.hp1 HG00738.hp1 others(39): Show |
intron_variant | MODIFIER | c.294+10121C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59470327 | ||||||
| chr15:59470397
|
A | C | 319 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(316): Show | 326 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(323): Show |
intron_variant | MODIFIER | c.294+10191A>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59470397 | ||||||
| chr15:59470611
|
T | C | 2 | a0001c0001t0001g0077a0001c0001t0001g0158 | 2 | NA18980.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.294+10405T>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59470611 | ||||||
| chr15:59470670
|
A | G | 9 | a0001c0001t0001g0286a0001c0001t0001g0363a0001c0002t0001g0011others(6): Show | 10 | HG01891.hp1 HG02622.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.294+10464A>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59470670 | ||||||
| chr15:59470699
|
A | T | 1 | a0001c0002t0001g0350 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.294+10493A>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59470699 | ||||||
| chr15:59470705
|
G | C | 1 | a0001c0002t0001g0350 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.294+10499G>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59470705 | ||||||
| chr15:59470751
|
C | T | 2 | a0001c0001t0001g0286a0001c0001t0001g0363 | 2 | HG02965.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.294+10545C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59470751 | ||||||
| chr15:59470772
|
T | C | 4 | a0001c0001t0001g0169a0001c0001t0001g0182a0001c0001t0001g0230others(1): Show | 4 | HG01109.hp2 HG02809.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.294+10566T>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59470772 | ||||||
| chr15:59470847
|
G | A | 1 | a0001c0002t0004g0015 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.294+10641G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59470847 | ||||||
| chr15:59471003
|
C | G | 1 | a0001c0001t0001g0360 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.294+10797C>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59471003 | ||||||
| chr15:59471069
|
C | T | 15 | a0001c0001t0001g0243a0001c0001t0001g0245a0001c0001t0001g0249others(12): Show | 15 | HG01109.hp1 HG01516.hp2 HG01993.hp2 others(12): Show |
intron_variant | MODIFIER | c.294+10863C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59471069 | ||||||
| chr15:59471255
|
C | T | 188 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(185): Show | 193 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(190): Show |
intron_variant | MODIFIER | c.294+11049C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59471255 | ||||||
| chr15:59471393
|
T | C | 7 | a0001c0002t0001g0011a0001c0002t0002g0050a0001c0002t0002g0145others(4): Show | 8 | HG01891.hp1 HG02622.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.294+11187T>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59471393 | ||||||
| chr15:59471493
|
A | T | 3 | a0001c0002t0004g0254a0001c0002t0008g0255a0001c0002t0008g0256 | 3 | NA18986.hp2 NA18989.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.294+11287A>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59471493 | ||||||
| chr15:59471543
|
G | A | 7 | a0001c0002t0001g0011a0001c0002t0002g0050a0001c0002t0002g0145others(4): Show | 8 | HG01891.hp1 HG02622.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.294+11337G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59471543 | ||||||
| chr15:59471545
|
G | A | 4 | a0001c0001t0001g0355a0001c0001t0001g0356a0001c0001t0001g0357others(1): Show | 4 | HG02818.hp2 HG02895.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.294+11339G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59471545 | ||||||
| chr15:59471637
|
A | AT | 302 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(299): Show | 309 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(306): Show |
intron_variant | MODIFIER | c.294+11443dupT | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr15 | 59471637 | |||||
| chr15:59471696
|
C | A | 3 | a0001c0001t0001g0187a0001c0001t0001g0190a0001c0001t0001g0199 | 3 | HG03834.hp1 HG04115.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.294+11490C>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59471696 | ||||||
| chr15:59471809
|
A | G | 1 | a0001c0001t0001g0179 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.294+11603A>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59471809 | ||||||
| chr15:59471931
|
A | G | 1 | a0001c0001t0001g0304 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.294+11725A>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59471931 | ||||||
| chr15:59471948
|
A | G | 105 | a0001c0001t0001g0046a0001c0001t0001g0129a0001c0001t0001g0148others(102): Show | 106 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.294+11742A>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59471948 | ||||||
| chr15:59472076
|
G | A | 1 | a0001c0002t0001g0053 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.294+11870G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59472076 | ||||||
| chr15:59472167
|
T | C | 304 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(301): Show | 311 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(308): Show |
intron_variant | MODIFIER | c.294+11961T>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59472167 | ||||||
| chr15:59472201
|
C | T | 1 | a0001c0001t0001g0360 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.294+11995C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59472201 | ||||||
| chr15:59472333
|
A | G | 1 | a0001c0001t0001g0221 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.294+12127A>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59472333 | ||||||
| chr15:59472492
|
C | G | 7 | a0001c0002t0001g0011a0001c0002t0002g0050a0001c0002t0002g0145others(4): Show | 8 | HG01891.hp1 HG02622.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.294+12286C>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59472492 | ||||||
| chr15:59472507
|
T | C | 182 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(179): Show | 187 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.294+12301T>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59472507 | ||||||
| chr15:59472513
|
T | G | 1 | a0001c0001t0001g0203 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.294+12307T>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59472513 | ||||||
| chr15:59472559
|
CT | C | 299 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(296): Show | 306 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(303): Show |
intron_variant | MODIFIER | c.294+12367delT | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr15 | 59472559 | |||||
| chr15:59472615
|
A | G | 17 | a0001c0001t0001g0243a0001c0001t0001g0245a0001c0001t0001g0249others(14): Show | 17 | HG01109.hp1 HG01516.hp2 HG01993.hp2 others(14): Show |
intron_variant | MODIFIER | c.294+12409A>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59472615 | ||||||
| chr15:59472706
|
A | G | 1 | a0001c0002t0012g0146 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.294+12500A>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59472706 | ||||||
| chr15:59472725
|
A | AT | 6 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0355others(3): Show | 6 | HG02818.hp2 HG02895.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.294+12525dupT | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr15 | 59472725 | |||||
| chr15:59472740
|
G | A | 319 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(316): Show | 326 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(323): Show |
intron_variant | MODIFIER | c.294+12534G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59472740 | ||||||
| chr15:59472746
|
C | A | 1 | a0001c0001t0001g0144 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.294+12540C>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59472746 | ||||||
| chr15:59472823
|
A | G | 1 | a0001c0001t0001g0109 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.294+12617A>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59472823 | ||||||
| chr15:59472996
|
T | C | 304 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(301): Show | 311 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(308): Show |
intron_variant | MODIFIER | c.294+12790T>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59472996 | ||||||
| chr15:59473704
|
C | A | 292 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(289): Show | 298 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(295): Show |
intron_variant | MODIFIER | c.294+13498C>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59473704 | ||||||
| chr15:59473777
|
G | A | 292 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(289): Show | 298 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(295): Show |
intron_variant | MODIFIER | c.294+13571G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59473777 | ||||||
| chr15:59473795
|
C | T | 304 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(301): Show | 311 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(308): Show |
intron_variant | MODIFIER | c.294+13589C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59473795 | ||||||
| chr15:59473843
|
T | C | 1 | a0001c0002t0013g0239 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.294+13637T>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59473843 | ||||||
| chr15:59473853
|
T | C | 5 | a0001c0001t0001g0065a0001c0001t0001g0088a0001c0001t0001g0089others(2): Show | 5 | HG00733.hp2 HG01358.hp1 HG01891.hp1 others(2): Show |
intron_variant | MODIFIER | c.294+13647T>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59473853 | ||||||
| chr15:59474000
|
T | G | 142 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(139): Show | 146 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(143): Show |
intron_variant | MODIFIER | c.294+13794T>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59474000 | ||||||
| chr15:59474050
|
G | A | 2 | a0001c0001t0001g0066a0001c0001t0001g0119 | 2 | HG00741.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.294+13844G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59474050 | ||||||
| chr15:59474070
|
C | T | 7 | a0001c0002t0001g0011a0001c0002t0002g0050a0001c0002t0002g0145others(4): Show | 8 | HG01891.hp1 HG02622.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.294+13864C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59474070 | ||||||
| chr15:59474078
|
C | T | 1 | a0001c0001t0001g0241 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.294+13872C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59474078 | ||||||
| chr15:59474246
|
C | T | 2 | a0001c0001t0001g0213a0001c0001t0001g0327 | 2 | HG03453.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.294+14040C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59474246 | ||||||
| chr15:59474317
|
A | G | 1 | a0001c0002t0001g0011 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.294+14111A>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59474317 | ||||||
| chr15:59474360
|
C | A | 2 | a0001c0001t0001g0144a0001c0002t0004g0015 | 2 | HG02647.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.294+14154C>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59474360 | ||||||
| chr15:59474404
|
A | G | 1 | a0001c0002t0013g0239 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.294+14198A>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59474404 | ||||||
| chr15:59474535
|
C | A | 1 | a0001c0001t0001g0186 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.294+14329C>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59474535 | ||||||
| chr15:59474557
|
T | C | 304 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(301): Show | 311 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(308): Show |
intron_variant | MODIFIER | c.294+14351T>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59474557 | ||||||
| chr15:59474668
|
C | T | 1 | a0001c0001t0001g0037 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.294+14462C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59474668 | ||||||
| chr15:59474762
|
T | C | 9 | a0001c0001t0001g0286a0001c0001t0001g0363a0001c0002t0001g0011others(6): Show | 10 | HG01891.hp1 HG02622.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.294+14556T>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59474762 | ||||||
| chr15:59475048
|
G | C | 1 | a0001c0001t0001g0315 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.294+14842G>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59475048 | ||||||
| chr15:59475247
|
T | C | 304 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(301): Show | 311 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(308): Show |
intron_variant | MODIFIER | c.294+15041T>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59475247 | ||||||
| chr15:59475276
|
C | G | 1 | a0001c0001t0001g0354 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.294+15070C>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59475276 | ||||||
| chr15:59475506
|
A | C | 3 | a0001c0002t0003g0225a0001c0002t0003g0228a0001c0002t0015g0227 | 3 | HG02486.hp1 HG02922.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.294+15300A>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59475506 | ||||||
| chr15:59475591
|
A | C | 1 | a0001c0001t0016g0166 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.294+15385A>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59475591 | ||||||
| chr15:59475736
|
A | G | 1 | a0001c0001t0001g0078 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.294+15530A>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59475736 | ||||||
| chr15:59475938
|
A | G | 7 | a0001c0002t0001g0011a0001c0002t0002g0050a0001c0002t0002g0145others(4): Show | 8 | HG01891.hp1 HG02622.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.294+15732A>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59475938 | ||||||
| chr15:59475947
|
G | A | 1 | a0001c0001t0001g0292 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.294+15741G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59475947 | ||||||
| chr15:59476016
|
T | C | 319 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(316): Show | 326 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(323): Show |
intron_variant | MODIFIER | c.294+15810T>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59476016 | ||||||
| chr15:59476225
|
AT | A | 9 | a0001c0001t0001g0080a0001c0001t0001g0116a0001c0001t0001g0155others(6): Show | 9 | HG01168.hp2 HG02523.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.295-16030delT | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr15 | 59476225 | |||||
| chr15:59476387
|
G | C | 319 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(316): Show | 326 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(323): Show |
intron_variant | MODIFIER | c.295-15884G>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59476387 | ||||||
| chr15:59476521
|
G | A | 1 | a0001c0001t0001g0293 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.295-15750G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59476521 | ||||||
| chr15:59476602
|
A | G | 45 | a0001c0001t0001g0009a0001c0001t0001g0154a0001c0001t0001g0178others(42): Show | 46 | HG00558.hp2 HG00733.hp1 HG00738.hp1 others(43): Show |
intron_variant | MODIFIER | c.295-15669A>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59476602 | ||||||
| chr15:59476651
|
C | T | 1 | a0001c0001t0001g0199 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.295-15620C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59476651 | ||||||
| chr15:59476653
|
G | A | 290 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(287): Show | 296 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(293): Show |
intron_variant | MODIFIER | c.295-15618G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59476653 | ||||||
| chr15:59476724
|
AG | A | 23 | a0001c0001t0001g0009a0001c0001t0001g0188a0001c0001t0001g0189others(20): Show | 24 | HG00558.hp2 HG01346.hp2 HG01928.hp2 others(21): Show |
intron_variant | MODIFIER | c.295-15545delG | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr15 | 59476724 | |||||
| chr15:59476736
|
G | A | 292 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(289): Show | 298 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(295): Show |
intron_variant | MODIFIER | c.295-15535G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59476736 | ||||||
| chr15:59476894
|
G | T | 2 | a0001c0001t0001g0065a0001c0001t0001g0090 | 2 | HG00733.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.295-15377G>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59476894 | ||||||
| chr15:59477051
|
C | T | 44 | a0001c0001t0001g0009a0001c0001t0001g0154a0001c0001t0001g0178others(41): Show | 45 | HG00558.hp2 HG00733.hp1 HG00738.hp1 others(42): Show |
intron_variant | MODIFIER | c.295-15220C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59477051 | ||||||
| chr15:59477057
|
T | G | 2 | a0001c0002t0010g0257a0001c0002t0010g0258 | 2 | HG03098.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.295-15214T>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59477057 | ||||||
| chr15:59477068
|
C | T | 44 | a0001c0001t0001g0009a0001c0001t0001g0154a0001c0001t0001g0178others(41): Show | 45 | HG00558.hp2 HG00733.hp1 HG00738.hp1 others(42): Show |
intron_variant | MODIFIER | c.295-15203C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59477068 | ||||||
| chr15:59477143
|
A | G | 44 | a0001c0001t0001g0009a0001c0001t0001g0154a0001c0001t0001g0178others(41): Show | 45 | HG00558.hp2 HG00733.hp1 HG00738.hp1 others(42): Show |
intron_variant | MODIFIER | c.295-15128A>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59477143 | ||||||
| chr15:59477162
|
A | T | 1 | a0001c0002t0012g0146 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.295-15109A>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59477162 | ||||||
| chr15:59477182
|
T | C | 1 | a0001c0001t0001g0288 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.295-15089T>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59477182 | ||||||
| chr15:59477262
|
A | C | 300 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(297): Show | 306 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(303): Show |
intron_variant | MODIFIER | c.295-15009A>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59477262 | ||||||
| chr15:59477343
|
C | T | 1 | a0001c0001t0001g0108 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.295-14928C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59477343 | ||||||
| chr15:59477344
|
G | A | 7 | a0001c0002t0001g0011a0001c0002t0002g0050a0001c0002t0002g0145others(4): Show | 8 | HG01891.hp1 HG02622.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.295-14927G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59477344 | ||||||
| chr15:59477361
|
G | C | 4 | a0001c0001t0001g0355a0001c0001t0001g0356a0001c0001t0001g0357others(1): Show | 4 | HG02818.hp2 HG02895.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.295-14910G>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59477361 | ||||||
| chr15:59477393
|
G | A | 3 | a0001c0001t0001g0040a0001c0002t0001g0029a0001c0002t0001g0041 | 3 | HG00099.hp1 HG00738.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.295-14878G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59477393 | ||||||
| chr15:59477702
|
A | G | 1 | a0001c0001t0001g0320 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.295-14569A>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59477702 | ||||||
| chr15:59477949
|
A | T | 1 | a0001c0002t0006g0047 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.295-14322A>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59477949 | ||||||
| chr15:59477980
|
C | G | 1 | a0001c0001t0001g0043 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.295-14291C>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59477980 | ||||||
| chr15:59478035
|
G | A | 234 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(231): Show | 239 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(236): Show |
intron_variant | MODIFIER | c.295-14236G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59478035 | ||||||
| chr15:59478203
|
C | T | 3 | a0001c0002t0005g0273a0001c0002t0005g0275a0001c0002t0005g0276 | 3 | HG02559.hp2 HG02723.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.295-14068C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59478203 | ||||||
| chr15:59478276
|
A | C | 3 | a0001c0001t0001g0231a0001c0001t0001g0234a0001c0001t0001g0235 | 3 | HG01243.hp2 HG02145.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.295-13995A>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59478276 | ||||||
| chr15:59478330
|
T | C | 1 | a0001c0001t0001g0344 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.295-13941T>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59478330 | ||||||
| chr15:59478377
|
C | G | 6 | a0001c0002t0002g0050a0001c0002t0002g0145a0001c0003t0002g0004others(3): Show | 7 | HG02622.hp1 HG02630.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.295-13894C>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59478377 | ||||||
| chr15:59478529
|
T | A | 1 | a0001c0001t0001g0226 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.295-13742T>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59478529 | ||||||
| chr15:59478577
|
C | T | 2 | a0001c0002t0001g0350a0001c0002t0013g0239 | 2 | HG02615.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.295-13694C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59478577 | ||||||
| chr15:59478702
|
C | T | 2 | a0001c0002t0001g0011a0001c0002t0003g0271 | 2 | HG01891.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.295-13569C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59478702 | ||||||
| chr15:59478703
|
G | A | 1 | a0001c0001t0001g0133 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.295-13568G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59478703 | ||||||
| chr15:59478757
|
CAG | C | 273 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(270): Show | 277 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(274): Show |
intron_variant | MODIFIER | c.295-13511_295-1351 others(6): Show |
FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr15 | 59478757 | |||||
| chr15:59479027
|
C | T | 2 | a0001c0001t0001g0269a0001c0001t0001g0287 | 2 | NA18989.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.295-13244C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59479027 | ||||||
| chr15:59479088
|
C | G | 2 | a0001c0002t0010g0257a0001c0002t0010g0258 | 2 | HG03098.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.295-13183C>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59479088 | ||||||
| chr15:59479226
|
T | G | 24 | a0001c0002t0001g0056a0001c0002t0001g0135a0001c0002t0001g0136others(21): Show | 26 | HG01109.hp1 HG01516.hp2 HG01993.hp2 others(23): Show |
intron_variant | MODIFIER | c.295-13045T>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59479226 | ||||||
| chr15:59479367
|
C | T | 1 | a0001c0001t0017g0220 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.295-12904C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59479367 | ||||||
| chr15:59479442
|
C | T | 1 | a0001c0001t0001g0065 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.295-12829C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59479442 | ||||||
| chr15:59479519
|
G | GA | 11 | a0001c0001t0001g0120a0001c0001t0001g0269a0001c0001t0001g0302others(8): Show | 12 | HG00323.hp1 HG00323.hp2 HG01978.hp2 others(9): Show |
intron_variant | MODIFIER | c.295-12729dupA | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr15 | 59479519 | |||||
| chr15:59479519
|
GA | G | 86 | a0001c0001t0001g0008a0001c0001t0001g0046a0001c0001t0001g0085others(83): Show | 87 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.295-12729delA | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr15 | 59479519 | |||||
| chr15:59479519
|
GAA | G | 147 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(144): Show | 151 | HG00099.hp2 HG00438.hp2 HG00558.hp1 others(148): Show |
intron_variant | MODIFIER | c.295-12730_295-1272 others(6): Show |
FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr15 | 59479519 | |||||
| chr15:59479519
|
GAAA | G | 19 | a0001c0001t0001g0107a0001c0002t0001g0056a0001c0002t0001g0135others(16): Show | 20 | HG01109.hp1 HG01516.hp2 HG01993.hp2 others(17): Show |
intron_variant | MODIFIER | c.295-12731_295-1272 others(7): Show |
FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr15 | 59479519 | |||||
| chr15:59479633
|
C | T | 1 | a0001c0001t0001g0144 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.295-12638C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59479633 | ||||||
| chr15:59479637
|
CA | C | 3 | a0001c0001t0001g0065a0001c0001t0001g0088a0001c0001t0001g0089 | 3 | HG01358.hp1 HG01891.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.295-12633delA | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59479637 | ||||||
| chr15:59479704
|
G | A | 2 | a0001c0002t0010g0257a0001c0002t0010g0258 | 2 | HG03098.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.295-12567G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59479704 | ||||||
| chr15:59479763
|
C | T | 18 | a0001c0002t0001g0056a0001c0002t0001g0135a0001c0002t0001g0136others(15): Show | 19 | HG01109.hp1 HG01516.hp2 HG01993.hp2 others(16): Show |
intron_variant | MODIFIER | c.295-12508C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59479763 | ||||||
| chr15:59479765
|
G | A | 1 | a0001c0001t0001g0327 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.295-12506G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59479765 | ||||||
| chr15:59479784
|
A | G | 2 | a0001c0002t0004g0015a0001c0002t0011g0010 | 3 | HG02647.hp1 HG02970.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.295-12487A>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59479784 | ||||||
| chr15:59479878
|
A | G | 1 | a0001c0002t0004g0015 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.295-12393A>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59479878 | ||||||
| chr15:59479951
|
G | A | 22 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0054others(19): Show | 24 | HG01081.hp2 HG01168.hp1 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.295-12320G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59479951 | ||||||
| chr15:59480011
|
A | G | 1 | a0001c0001t0019g0223 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.295-12260A>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59480011 | ||||||
| chr15:59480016
|
A | G | 24 | a0001c0002t0001g0056a0001c0002t0001g0135a0001c0002t0001g0136others(21): Show | 26 | HG01109.hp1 HG01516.hp2 HG01993.hp2 others(23): Show |
intron_variant | MODIFIER | c.295-12255A>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59480016 | ||||||
| chr15:59480568
|
G | A | 1 | a0001c0001t0001g0322 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.295-11703G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59480568 | ||||||
| chr15:59480608
|
T | C | 3 | a0001c0001t0001g0187a0001c0001t0001g0190a0001c0001t0001g0199 | 3 | HG03834.hp1 HG04115.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.295-11663T>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59480608 | ||||||
| chr15:59480692
|
G | A | 2 | a0001c0002t0001g0350a0001c0002t0013g0239 | 2 | HG02615.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.295-11579G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59480692 | ||||||
| chr15:59480873
|
T | C | 3 | a0001c0002t0001g0021a0001c0002t0001g0022a0001c0002t0001g0031 | 3 | HG02602.hp2 HG02698.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.295-11398T>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59480873 | ||||||
| chr15:59481002
|
A | T | 6 | a0001c0002t0002g0050a0001c0002t0002g0145a0001c0003t0002g0004others(3): Show | 7 | HG02622.hp1 HG02630.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.295-11269A>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59481002 | ||||||
| chr15:59481151
|
C | G | 1 | a0001c0002t0001g0026 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.295-11120C>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59481151 | ||||||
| chr15:59481293
|
C | T | 1 | a0001c0001t0001g0186 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.295-10978C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59481293 | ||||||
| chr15:59481436
|
C | A | 315 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(312): Show | 321 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(318): Show |
intron_variant | MODIFIER | c.295-10835C>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59481436 | ||||||
| chr15:59481800
|
A | G | 2 | a0001c0001t0001g0093a0001c0001t0001g0106 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.295-10471A>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59481800 | ||||||
| chr15:59481865
|
A | C | 19 | a0001c0002t0001g0056a0001c0002t0001g0135a0001c0002t0001g0136others(16): Show | 20 | HG01109.hp1 HG01516.hp2 HG01993.hp2 others(17): Show |
intron_variant | MODIFIER | c.295-10406A>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59481865 | ||||||
| chr15:59481965
|
TAG | T | 6 | a0001c0002t0002g0050a0001c0002t0002g0145a0001c0003t0002g0004others(3): Show | 7 | HG02622.hp1 HG02630.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.295-10304_295-1030 others(6): Show |
FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr15 | 59481965 | |||||
| chr15:59482007
|
T | G | 1 | a0001c0001t0001g0332 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.295-10264T>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59482007 | ||||||
| chr15:59482014
|
A | G | 1 | a0001c0001t0001g0105 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.295-10257A>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59482014 | ||||||
| chr15:59482263
|
G | A | 64 | a0001c0001t0001g0009a0001c0001t0001g0019a0001c0001t0001g0077others(61): Show | 65 | HG00558.hp2 HG00738.hp1 HG01081.hp1 others(62): Show |
intron_variant | MODIFIER | c.295-10008G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59482263 | ||||||
| chr15:59482344
|
C | G | 2 | a0001c0001t0001g0155a0001c0001t0001g0156 | 2 | HG02976.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.295-9927C>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59482344 | ||||||
| chr15:59482377
|
T | G | 13 | a0001c0001t0001g0008a0001c0001t0001g0067a0001c0001t0001g0085others(10): Show | 14 | HG00423.hp1 HG01256.hp2 HG01258.hp2 others(11): Show |
intron_variant | MODIFIER | c.295-9894T>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59482377 | ||||||
| chr15:59482417
|
C | T | 1 | a0001c0001t0001g0219 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.295-9854C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59482417 | ||||||
| chr15:59482555
|
C | T | 1 | a0001c0001t0001g0305 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.295-9716C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59482555 | ||||||
| chr15:59482822
|
C | T | 1 | a0001c0001t0001g0217 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.295-9449C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59482822 | ||||||
| chr15:59482823
|
G | A | 20 | a0001c0002t0001g0056a0001c0002t0001g0248a0001c0002t0001g0330others(17): Show | 21 | HG01109.hp1 HG01516.hp2 HG01993.hp2 others(18): Show |
intron_variant | MODIFIER | c.295-9448G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59482823 | ||||||
| chr15:59482873
|
G | C | 10 | a0001c0001t0001g0245a0001c0001t0001g0261a0001c0001t0001g0262others(7): Show | 10 | HG00544.hp1 HG02809.hp1 NA18939.hp2 others(7): Show |
intron_variant | MODIFIER | c.295-9398G>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59482873 | ||||||
| chr15:59482918
|
ATT | A | 9 | a0001c0002t0001g0056a0001c0002t0001g0248a0001c0002t0004g0244others(6): Show | 9 | HG01109.hp1 HG01516.hp2 HG01993.hp2 others(6): Show |
intron_variant | MODIFIER | c.295-9350_295-9349d others(4): Show |
FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr15 | 59482918 | |||||
| chr15:59483227
|
G | A | 1 | a0001c0001t0001g0116 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.295-9044G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59483227 | ||||||
| chr15:59483261
|
A | C | 1 | a0001c0002t0007g0138 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.295-9010A>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59483261 | ||||||
| chr15:59483284
|
G | A | 1 | a0001c0001t0001g0043 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.295-8987G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59483284 | ||||||
| chr15:59483306
|
G | A | 280 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(277): Show | 286 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(283): Show |
intron_variant | MODIFIER | c.295-8965G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59483306 | ||||||
| chr15:59483333
|
G | A | 1 | a0001c0001t0001g0344 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.295-8938G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59483333 | ||||||
| chr15:59483407
|
T | G | 1 | a0001c0001t0001g0182 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.295-8864T>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59483407 | ||||||
| chr15:59483465
|
A | G | 46 | a0001c0001t0001g0147a0001c0002t0001g0011a0001c0002t0001g0056others(43): Show | 48 | HG01109.hp1 HG01516.hp2 HG01884.hp2 others(45): Show |
intron_variant | MODIFIER | c.295-8806A>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59483465 | ||||||
| chr15:59483553
|
A | G | 1 | a0001c0001t0001g0064 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.295-8718A>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59483553 | ||||||
| chr15:59483695
|
A | G | 4 | a0001c0001t0001g0324a0001c0001t0001g0325a0001c0001t0001g0339others(1): Show | 4 | HG02109.hp1 HG03195.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.295-8576A>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59483695 | ||||||
| chr15:59483903
|
A | G | 2 | a0001c0001t0001g0212a0001c0001t0001g0213 | 2 | NA19065.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.295-8368A>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59483903 | ||||||
| chr15:59484037
|
A | G | 1 | a0001c0002t0001g0053 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.295-8234A>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59484037 | ||||||
| chr15:59484053
|
A | G | 23 | a0001c0001t0001g0147a0001c0002t0001g0011a0001c0002t0003g0139others(20): Show | 24 | HG01884.hp2 HG01891.hp1 HG02258.hp1 others(21): Show |
intron_variant | MODIFIER | c.295-8218A>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59484053 | ||||||
| chr15:59484236
|
T | C | 1 | a0001c0001t0001g0294 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.295-8035T>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59484236 | ||||||
| chr15:59484397
|
A | T | 25 | a0001c0002t0001g0056a0001c0002t0001g0135a0001c0002t0001g0136others(22): Show | 27 | HG01109.hp1 HG01516.hp2 HG01993.hp2 others(24): Show |
intron_variant | MODIFIER | c.295-7874A>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59484397 | ||||||
| chr15:59484473
|
C | T | 25 | a0001c0002t0001g0056a0001c0002t0001g0135a0001c0002t0001g0136others(22): Show | 27 | HG01109.hp1 HG01516.hp2 HG01993.hp2 others(24): Show |
intron_variant | MODIFIER | c.295-7798C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59484473 | ||||||
| chr15:59484503
|
C | T | 1 | a0001c0002t0002g0050 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.295-7768C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59484503 | ||||||
| chr15:59484575
|
T | C | 1 | a0001c0001t0001g0083 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.295-7696T>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59484575 | ||||||
| chr15:59484696
|
C | T | 21 | a0001c0002t0001g0056a0001c0002t0001g0248a0001c0002t0001g0330others(18): Show | 23 | HG01109.hp1 HG01516.hp2 HG01993.hp2 others(20): Show |
intron_variant | MODIFIER | c.295-7575C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59484696 | ||||||
| chr15:59484717
|
T | C | 25 | a0001c0002t0001g0056a0001c0002t0001g0135a0001c0002t0001g0136others(22): Show | 27 | HG01109.hp1 HG01516.hp2 HG01993.hp2 others(24): Show |
intron_variant | MODIFIER | c.295-7554T>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59484717 | ||||||
| chr15:59484719
|
T | C | 25 | a0001c0002t0001g0056a0001c0002t0001g0135a0001c0002t0001g0136others(22): Show | 27 | HG01109.hp1 HG01516.hp2 HG01993.hp2 others(24): Show |
intron_variant | MODIFIER | c.295-7552T>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59484719 | ||||||
| chr15:59484720
|
C | A | 11 | a0001c0001t0001g0154a0001c0001t0001g0181a0001c0001t0001g0186others(8): Show | 11 | HG00738.hp1 HG02015.hp1 HG02027.hp2 others(8): Show |
intron_variant | MODIFIER | c.295-7551C>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59484720 | ||||||
| chr15:59484729
|
G | A | 1 | a0001c0001t0001g0075 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.295-7542G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59484729 | ||||||
| chr15:59484891
|
C | T | 1 | a0001c0002t0001g0248 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.295-7380C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59484891 | ||||||
| chr15:59485013
|
C | T | 1 | a0001c0002t0010g0258 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.295-7258C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59485013 | ||||||
| chr15:59485067
|
G | C | 1 | a0001c0001t0001g0095 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.295-7204G>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59485067 | ||||||
| chr15:59485247
|
G | T | 24 | a0001c0002t0001g0056a0001c0002t0001g0135a0001c0002t0001g0136others(21): Show | 26 | HG01109.hp1 HG01516.hp2 HG01993.hp2 others(23): Show |
intron_variant | MODIFIER | c.295-7024G>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59485247 | ||||||
| chr15:59485271
|
C | T | 1 | a0001c0002t0014g0140 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.295-7000C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59485271 | ||||||
| chr15:59485421
|
A | C | 25 | a0001c0002t0001g0056a0001c0002t0001g0135a0001c0002t0001g0136others(22): Show | 27 | HG01109.hp1 HG01516.hp2 HG01993.hp2 others(24): Show |
intron_variant | MODIFIER | c.295-6850A>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59485421 | ||||||
| chr15:59485950
|
G | A | 2 | a0001c0002t0003g0139a0001c0002t0014g0140 | 2 | HG02451.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.295-6321G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59485950 | ||||||
| chr15:59486007
|
C | T | 5 | a0001c0001t0001g0289a0001c0001t0001g0311a0001c0001t0001g0315others(2): Show | 5 | HG01361.hp2 HG01978.hp1 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.295-6264C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59486007 | ||||||
| chr15:59486025
|
G | A | 24 | a0001c0002t0001g0056a0001c0002t0001g0135a0001c0002t0001g0136others(21): Show | 26 | HG01109.hp1 HG01516.hp2 HG01993.hp2 others(23): Show |
intron_variant | MODIFIER | c.295-6246G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59486025 | ||||||
| chr15:59486157
|
C | G | 1 | a0001c0002t0001g0350 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.295-6114C>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59486157 | ||||||
| chr15:59486175
|
G | GAAGA | 45 | a0001c0002t0001g0011a0001c0002t0001g0056a0001c0002t0001g0135others(42): Show | 47 | HG01109.hp1 HG01516.hp2 HG01884.hp2 others(44): Show |
intron_variant | MODIFIER | c.295-6084_295-6081d others(6): Show |
FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr15 | 59486175 | |||||
| chr15:59486238
|
G | A | 3 | a0001c0001t0001g0324a0001c0001t0001g0325a0001c0001t0001g0339 | 3 | HG02109.hp1 HG03195.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.295-6033G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59486238 | ||||||
| chr15:59486347
|
G | A | 45 | a0001c0002t0001g0011a0001c0002t0001g0056a0001c0002t0001g0135others(42): Show | 47 | HG01109.hp1 HG01516.hp2 HG01884.hp2 others(44): Show |
intron_variant | MODIFIER | c.295-5924G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59486347 | ||||||
| chr15:59486464
|
T | C | 3 | a0001c0001t0001g0355a0001c0001t0001g0357a0001c0001t0001g0358 | 3 | HG02818.hp2 HG06807.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.295-5807T>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59486464 | ||||||
| chr15:59486542
|
C | T | 25 | a0001c0002t0001g0056a0001c0002t0001g0135a0001c0002t0001g0136others(22): Show | 27 | HG01109.hp1 HG01516.hp2 HG01993.hp2 others(24): Show |
intron_variant | MODIFIER | c.295-5729C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59486542 | ||||||
| chr15:59486656
|
A | G | 25 | a0001c0002t0001g0056a0001c0002t0001g0135a0001c0002t0001g0136others(22): Show | 27 | HG01109.hp1 HG01516.hp2 HG01993.hp2 others(24): Show |
intron_variant | MODIFIER | c.295-5615A>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59486656 | ||||||
| chr15:59486663
|
A | C | 284 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(281): Show | 291 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(288): Show |
intron_variant | MODIFIER | c.295-5608A>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59486663 | ||||||
| chr15:59486701
|
T | C | 2 | a0001c0002t0001g0135a0001c0002t0001g0136 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.295-5570T>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59486701 | ||||||
| chr15:59486727
|
C | A | 19 | a0001c0002t0001g0056a0001c0002t0001g0135a0001c0002t0001g0136others(16): Show | 20 | HG01109.hp1 HG01516.hp2 HG01993.hp2 others(17): Show |
intron_variant | MODIFIER | c.295-5544C>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59486727 | ||||||
| chr15:59486756
|
A | G | 2 | a0001c0002t0001g0020a0001c0002t0001g0048 | 2 | HG02015.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.295-5515A>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59486756 | ||||||
| chr15:59486957
|
T | G | 25 | a0001c0002t0001g0056a0001c0002t0001g0135a0001c0002t0001g0136others(22): Show | 27 | HG01109.hp1 HG01516.hp2 HG01993.hp2 others(24): Show |
intron_variant | MODIFIER | c.295-5314T>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59486957 | ||||||
| chr15:59487006
|
T | C | 1 | a0001c0002t0001g0031 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.295-5265T>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59487006 | ||||||
| chr15:59487053
|
G | A | 4 | a0001c0001t0001g0063a0001c0001t0001g0091a0001c0001t0001g0092others(1): Show | 4 | HG01069.hp1 HG01071.hp2 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.295-5218G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59487053 | ||||||
| chr15:59487117
|
C | G | 21 | a0001c0001t0001g0182a0001c0002t0001g0011a0001c0002t0003g0139others(18): Show | 21 | HG01884.hp2 HG01891.hp1 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.295-5154C>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59487117 | ||||||
| chr15:59487145
|
TTAAAG | T | 172 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(169): Show | 177 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(174): Show |
intron_variant | MODIFIER | c.295-5123_295-5119d others(7): Show |
FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr15 | 59487145 | |||||
| chr15:59487173
|
AAT | A | 317 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(314): Show | 324 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(321): Show |
intron_variant | MODIFIER | c.295-5085_295-5084d others(4): Show |
FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr15 | 59487173 | |||||
| chr15:59487256
|
GT | G | 25 | a0001c0002t0001g0056a0001c0002t0001g0135a0001c0002t0001g0136others(22): Show | 27 | HG01109.hp1 HG01516.hp2 HG01993.hp2 others(24): Show |
intron_variant | MODIFIER | c.295-5009delT | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr15 | 59487256 | |||||
| chr15:59487335
|
G | A | 25 | a0001c0002t0001g0056a0001c0002t0001g0135a0001c0002t0001g0136others(22): Show | 27 | HG01109.hp1 HG01516.hp2 HG01993.hp2 others(24): Show |
intron_variant | MODIFIER | c.295-4936G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59487335 | ||||||
| chr15:59487373
|
GCAAAC | G | 25 | a0001c0002t0001g0056a0001c0002t0001g0135a0001c0002t0001g0136others(22): Show | 27 | HG01109.hp1 HG01516.hp2 HG01993.hp2 others(24): Show |
intron_variant | MODIFIER | c.295-4891_295-4887d others(7): Show |
FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr15 | 59487373 | |||||
| chr15:59487431
|
A | T | 1 | a0001c0002t0001g0011 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.295-4840A>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59487431 | ||||||
| chr15:59487448
|
T | A | 25 | a0001c0002t0001g0056a0001c0002t0001g0135a0001c0002t0001g0136others(22): Show | 27 | HG01109.hp1 HG01516.hp2 HG01993.hp2 others(24): Show |
intron_variant | MODIFIER | c.295-4823T>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59487448 | ||||||
| chr15:59487516
|
A | G | 18 | a0001c0002t0001g0056a0001c0002t0001g0135a0001c0002t0001g0136others(15): Show | 19 | HG01109.hp1 HG01516.hp2 HG01993.hp2 others(16): Show |
intron_variant | MODIFIER | c.295-4755A>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59487516 | ||||||
| chr15:59487938
|
CAAAACA | C | 6 | a0001c0001t0001g0151a0001c0001t0001g0160a0001c0001t0001g0162others(3): Show | 6 | HG02132.hp1 NA18957.hp1 NA18960.hp2 others(3): Show |
intron_variant | MODIFIER | c.295-4319_295-4314d others(8): Show |
FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr15 | 59487938 | |||||
| chr15:59487944
|
AAAAAC | A | 25 | a0001c0002t0001g0056a0001c0002t0001g0135a0001c0002t0001g0136others(22): Show | 27 | HG01109.hp1 HG01516.hp2 HG01993.hp2 others(24): Show |
intron_variant | MODIFIER | c.295-4322_295-4318d others(7): Show |
FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr15 | 59487944 | |||||
| chr15:59487961
|
C | A | 19 | a0001c0002t0001g0056a0001c0002t0001g0135a0001c0002t0001g0136others(16): Show | 20 | HG01109.hp1 HG01516.hp2 HG01993.hp2 others(17): Show |
intron_variant | MODIFIER | c.295-4310C>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59487961 | ||||||
| chr15:59487979
|
A | G | 1 | a0001c0002t0001g0350 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.295-4292A>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59487979 | ||||||
| chr15:59488117
|
T | C | 1 | a0001c0001t0001g0356 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.295-4154T>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59488117 | ||||||
| chr15:59488163
|
C | G | 1 | a0004c0008t0001g0309 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.295-4108C>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59488163 | ||||||
| chr15:59488287
|
A | T | 3 | a0001c0001t0001g0071a0001c0001t0001g0198a0001c0001t0001g0272 | 3 | HG02056.hp1 HG02071.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.295-3984A>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59488287 | ||||||
| chr15:59488473
|
A | T | 25 | a0001c0002t0001g0056a0001c0002t0001g0135a0001c0002t0001g0136others(22): Show | 27 | HG01109.hp1 HG01516.hp2 HG01993.hp2 others(24): Show |
intron_variant | MODIFIER | c.295-3798A>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59488473 | ||||||
| chr15:59488500
|
T | A | 3 | a0001c0002t0001g0135a0001c0002t0001g0136a0001c0002t0012g0146 | 3 | HG02895.hp1 HG02897.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.295-3771T>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59488500 | ||||||
| chr15:59488670
|
A | G | 1 | a0001c0001t0001g0320 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.295-3601A>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59488670 | ||||||
| chr15:59488822
|
C | T | 2 | a0001c0002t0001g0224a0001c0002t0001g0330 | 2 | HG02809.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.295-3449C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59488822 | ||||||
| chr15:59488839
|
G | A | 1 | a0001c0001t0001g0186 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.295-3432G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59488839 | ||||||
| chr15:59488923
|
A | G | 1 | a0001c0001t0001g0133 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.295-3348A>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59488923 | ||||||
| chr15:59488946
|
C | T | 7 | a0001c0001t0001g0231a0001c0001t0001g0232a0001c0001t0001g0233others(4): Show | 7 | HG01243.hp2 HG01515.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.295-3325C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59488946 | ||||||
| chr15:59489040
|
C | T | 6 | a0001c0002t0002g0050a0001c0002t0002g0145a0001c0003t0002g0004others(3): Show | 7 | HG02622.hp1 HG02630.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.295-3231C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59489040 | ||||||
| chr15:59489047
|
C | T | 1 | a0001c0001t0001g0055 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.295-3224C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59489047 | ||||||
| chr15:59489053
|
C | T | 1 | a0001c0001t0001g0336 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.295-3218C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59489053 | ||||||
| chr15:59489068
|
A | G | 315 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(312): Show | 321 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(318): Show |
intron_variant | MODIFIER | c.295-3203A>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59489068 | ||||||
| chr15:59489081
|
C | T | 15 | a0001c0002t0001g0035a0001c0002t0001g0036a0001c0002t0001g0056others(12): Show | 16 | HG01109.hp1 HG01515.hp2 HG01516.hp2 others(13): Show |
intron_variant | MODIFIER | c.295-3190C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59489081 | ||||||
| chr15:59489137
|
C | T | 1 | a0001c0002t0001g0350 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.295-3134C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59489137 | ||||||
| chr15:59489147
|
C | T | 25 | a0001c0002t0001g0056a0001c0002t0001g0135a0001c0002t0001g0136others(22): Show | 27 | HG01109.hp1 HG01516.hp2 HG01993.hp2 others(24): Show |
intron_variant | MODIFIER | c.295-3124C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59489147 | ||||||
| chr15:59489222
|
G | A | 2 | a0001c0001t0001g0087a0001c0001t0001g0096 | 2 | HG02257.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.295-3049G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59489222 | ||||||
| chr15:59489252
|
G | A | 194 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(191): Show | 197 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(194): Show |
intron_variant | MODIFIER | c.295-3019G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59489252 | ||||||
| chr15:59489266
|
A | AATAC | 4 | a0001c0001t0001g0191a0001c0002t0001g0011a0001c0002t0001g0023others(1): Show | 4 | HG00642.hp1 HG01891.hp1 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.295-2961_295-2958d others(6): Show |
FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr15 | 59489266 | |||||
| chr15:59489266
|
A | C | 2 | a0001c0001t0001g0301a0001c0001t0001g0326 | 2 | HG02258.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.295-3005A>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59489266 | ||||||
| chr15:59489266
|
AATAC | A | 251 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(248): Show | 255 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(252): Show |
intron_variant | MODIFIER | c.295-2961_295-2958d others(6): Show |
FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr15 | 59489266 | |||||
| chr15:59489266
|
AATACATA others(1): Show |
A | 4 | a0001c0001t0001g0161a0001c0001t0001g0163a0001c0001t0001g0320others(1): Show | 4 | HG02622.hp2 HG02896.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.295-2965_295-2958d others(10): Show |
FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr15 | 59489266 | |||||
| chr15:59489266
|
AATACATA others(5): Show |
A | 1 | a0001c0001t0001g0082 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.295-2969_295-2958d others(14): Show |
FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr15 | 59489266 | |||||
| chr15:59489298
|
C | CATACATA others(5): Show |
6 | a0001c0002t0002g0145a0001c0002t0012g0146a0001c0003t0002g0004others(3): Show | 7 | HG02622.hp1 HG02630.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.295-2962_295-2961i others(14): Show |
FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr15 | 59489298 | |||||
| chr15:59489306
|
C | T | 2 | a0001c0002t0004g0015a0001c0002t0011g0010 | 3 | HG02647.hp1 HG02970.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.295-2965C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59489306 | ||||||
| chr15:59489310
|
C | T | 10 | a0001c0002t0001g0056a0001c0002t0001g0248a0001c0002t0004g0244others(7): Show | 10 | HG01109.hp1 HG01516.hp2 HG01993.hp2 others(7): Show |
intron_variant | MODIFIER | c.295-2961C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59489310 | ||||||
| chr15:59489310
|
CATAT | C | 2 | a0001c0002t0004g0015a0001c0002t0011g0010 | 3 | HG02647.hp1 HG02970.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.295-2957_295-2954d others(6): Show |
FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr15 | 59489310 | |||||
| chr15:59489314
|
T | C | 23 | a0001c0001t0001g0039a0001c0002t0001g0056a0001c0002t0001g0135others(20): Show | 24 | HG01109.hp1 HG01516.hp2 HG01993.hp2 others(21): Show |
intron_variant | MODIFIER | c.295-2957T>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59489314 | ||||||
| chr15:59489314
|
TATAC | T | 8 | a0001c0001t0001g0002a0001c0001t0001g0025a0001c0001t0001g0030others(5): Show | 9 | HG00735.hp1 HG00741.hp2 HG01255.hp1 others(6): Show |
intron_variant | MODIFIER | c.295-2940_295-2937d others(6): Show |
FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr15 | 59489314 | |||||
| chr15:59489318
|
C | T | 2 | a0001c0001t0001g0039a0001c0001t0001g0338 | 2 | HG03041.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.295-2953C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59489318 | ||||||
| chr15:59489412
|
CAT | C | 4 | a0001c0001t0001g0090a0001c0001t0001g0178a0001c0001t0001g0179others(1): Show | 4 | HG00733.hp1 HG00733.hp2 HG01168.hp2 others(1): Show |
intron_variant | MODIFIER | c.295-2857_295-2856d others(4): Show |
FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr15 | 59489412 | |||||
| chr15:59489569
|
C | T | 41 | a0001c0002t0001g0011a0001c0002t0001g0056a0001c0002t0001g0135others(38): Show | 43 | HG01109.hp1 HG01516.hp2 HG01884.hp2 others(40): Show |
intron_variant | MODIFIER | c.295-2702C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59489569 | ||||||
| chr15:59489736
|
C | T | 1 | a0001c0001t0001g0162 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.295-2535C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59489736 | ||||||
| chr15:59489790
|
G | T | 1 | a0001c0002t0001g0053 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.295-2481G>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59489790 | ||||||
| chr15:59489865
|
G | T | 26 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0016others(23): Show | 29 | HG00735.hp1 HG00741.hp2 HG01074.hp2 others(26): Show |
intron_variant | MODIFIER | c.295-2406G>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59489865 | ||||||
| chr15:59490129
|
A | C | 4 | a0001c0002t0005g0273a0001c0002t0005g0274a0001c0002t0005g0275others(1): Show | 4 | HG02559.hp2 HG02723.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.295-2142A>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59490129 | ||||||
| chr15:59490187
|
C | T | 2 | a0001c0001t0001g0172a0001c0001t0001g0327 | 2 | HG01192.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.295-2084C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59490187 | ||||||
| chr15:59490392
|
A | G | 26 | a0001c0002t0001g0056a0001c0002t0001g0135a0001c0002t0001g0136others(23): Show | 28 | HG01109.hp1 HG01516.hp2 HG01993.hp2 others(25): Show |
intron_variant | MODIFIER | c.295-1879A>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59490392 | ||||||
| chr15:59490396
|
G | GAA | 26 | a0001c0002t0001g0056a0001c0002t0001g0135a0001c0002t0001g0136others(23): Show | 28 | HG01109.hp1 HG01516.hp2 HG01993.hp2 others(25): Show |
intron_variant | MODIFIER | c.295-1869_295-1868d others(4): Show |
FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr15 | 59490396 | |||||
| chr15:59490562
|
C | T | 20 | a0001c0002t0001g0056a0001c0002t0001g0135a0001c0002t0001g0136others(17): Show | 21 | HG01109.hp1 HG01516.hp2 HG01993.hp2 others(18): Show |
intron_variant | MODIFIER | c.295-1709C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59490562 | ||||||
| chr15:59490743
|
T | C | 20 | a0001c0002t0001g0056a0001c0002t0001g0135a0001c0002t0001g0136others(17): Show | 21 | HG01109.hp1 HG01516.hp2 HG01993.hp2 others(18): Show |
intron_variant | MODIFIER | c.295-1528T>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59490743 | ||||||
| chr15:59490758
|
T | C | 315 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(312): Show | 321 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(318): Show |
intron_variant | MODIFIER | c.295-1513T>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59490758 | ||||||
| chr15:59490794
|
C | T | 20 | a0001c0002t0001g0056a0001c0002t0001g0135a0001c0002t0001g0136others(17): Show | 21 | HG01109.hp1 HG01516.hp2 HG01993.hp2 others(18): Show |
intron_variant | MODIFIER | c.295-1477C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59490794 | ||||||
| chr15:59491309
|
C | A | 1 | a0001c0002t0004g0015 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.295-962C>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59491309 | ||||||
| chr15:59491337
|
T | C | 2 | a0001c0002t0005g0236a0001c0002t0005g0359 | 2 | HG02258.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.295-934T>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59491337 | ||||||
| chr15:59491426
|
T | C | 7 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0243others(4): Show | 7 | NA18943.hp2 NA18952.hp1 NA18957.hp2 others(4): Show |
intron_variant | MODIFIER | c.295-845T>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59491426 | ||||||
| chr15:59491455
|
A | C | 1 | a0001c0001t0001g0288 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.295-816A>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59491455 | ||||||
| chr15:59491523
|
T | C | 1 | a0001c0001t0001g0181 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.295-748T>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59491523 | ||||||
| chr15:59491577
|
G | T | 20 | a0001c0002t0001g0056a0001c0002t0001g0135a0001c0002t0001g0136others(17): Show | 21 | HG01109.hp1 HG01516.hp2 HG01993.hp2 others(18): Show |
intron_variant | MODIFIER | c.295-694G>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59491577 | ||||||
| chr15:59491640
|
T | A | 1 | a0001c0001t0001g0079 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.295-631T>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59491640 | ||||||
| chr15:59491652
|
C | T | 20 | a0001c0002t0001g0056a0001c0002t0001g0135a0001c0002t0001g0136others(17): Show | 21 | HG01109.hp1 HG01516.hp2 HG01993.hp2 others(18): Show |
intron_variant | MODIFIER | c.295-619C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59491652 | ||||||
| chr15:59491655
|
G | A | 1 | a0001c0001t0001g0098 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.295-616G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59491655 | ||||||
| chr15:59491721
|
T | G | 20 | a0001c0002t0001g0056a0001c0002t0001g0135a0001c0002t0001g0136others(17): Show | 21 | HG01109.hp1 HG01516.hp2 HG01993.hp2 others(18): Show |
intron_variant | MODIFIER | c.295-550T>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59491721 | ||||||
| chr15:59491944
|
C | T | 1 | a0001c0002t0012g0146 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.295-327C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59491944 | ||||||
| chr15:59491965
|
C | CA | 6 | a0001c0002t0002g0050a0001c0002t0002g0145a0001c0003t0002g0004others(3): Show | 7 | HG02622.hp1 HG02630.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.295-296dupA | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr15 | 59491965 | |||||
| chr15:59491970
|
AAAAAAG | A | 20 | a0001c0002t0001g0056a0001c0002t0001g0135a0001c0002t0001g0136others(17): Show | 21 | HG01109.hp1 HG01516.hp2 HG01993.hp2 others(18): Show |
intron_variant | MODIFIER | c.295-295_295-290del others(6): Show |
FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr15 | 59491970 | |||||
| chr15:59492135
|
C | A | 301 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(298): Show | 308 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(305): Show |
intron_variant | MODIFIER | c.295-136C>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 3/8 | chr15 | 59492135 | ||||||
| chr15:59492449
|
A | G | 191 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(188): Show | 197 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(194): Show |
intron_variant | MODIFIER | c.413+60A>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59492449 | ||||||
| chr15:59492527
|
T | C | 17 | a0001c0002t0001g0056a0001c0002t0001g0135a0001c0002t0001g0136others(14): Show | 18 | HG01109.hp1 HG01516.hp2 HG01993.hp2 others(15): Show |
intron_variant | MODIFIER | c.413+138T>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59492527 | ||||||
| chr15:59492586
|
C | T | 1 | a0001c0001t0001g0027 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.413+197C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59492586 | ||||||
| chr15:59492590
|
A | G | 1 | a0001c0001t0001g0321 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.413+201A>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59492590 | ||||||
| chr15:59492667
|
A | T | 19 | a0001c0002t0001g0056a0001c0002t0001g0135a0001c0002t0001g0136others(16): Show | 20 | HG01109.hp1 HG01516.hp2 HG01993.hp2 others(17): Show |
intron_variant | MODIFIER | c.413+278A>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59492667 | ||||||
| chr15:59492755
|
T | C | 1 | a0001c0001t0001g0329 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.413+366T>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59492755 | ||||||
| chr15:59492759
|
G | A | 1 | a0001c0001t0001g0329 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.413+370G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59492759 | ||||||
| chr15:59492760
|
G | T | 9 | a0001c0001t0001g0154a0001c0001t0001g0186a0001c0001t0001g0191others(6): Show | 9 | HG02015.hp1 HG02027.hp2 HG02523.hp2 others(6): Show |
intron_variant | MODIFIER | c.413+371G>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59492760 | ||||||
| chr15:59492845
|
T | C | 2 | a0001c0002t0001g0350a0001c0002t0013g0239 | 2 | HG02615.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.413+456T>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59492845 | ||||||
| chr15:59492869
|
C | T | 8 | a0001c0001t0001g0150a0001c0001t0001g0161a0001c0001t0001g0163others(5): Show | 8 | HG02280.hp2 HG02622.hp2 HG02698.hp2 others(5): Show |
intron_variant | MODIFIER | c.413+480C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59492869 | ||||||
| chr15:59492918
|
A | C | 2 | a0001c0002t0001g0350a0001c0002t0013g0239 | 2 | HG02615.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.413+529A>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59492918 | ||||||
| chr15:59492976
|
G | A | 1 | a0001c0002t0001g0053 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.413+587G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59492976 | ||||||
| chr15:59493175
|
G | C | 1 | a0001c0001t0001g0178 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.413+786G>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59493175 | ||||||
| chr15:59493183
|
G | C | 1 | a0001c0001t0001g0322 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.413+794G>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59493183 | ||||||
| chr15:59493201
|
T | A | 19 | a0001c0002t0001g0056a0001c0002t0001g0135a0001c0002t0001g0136others(16): Show | 20 | HG01109.hp1 HG01516.hp2 HG01993.hp2 others(17): Show |
intron_variant | MODIFIER | c.413+812T>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59493201 | ||||||
| chr15:59493207
|
C | T | 1 | a0001c0001t0001g0327 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.413+818C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59493207 | ||||||
| chr15:59493260
|
G | A | 311 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(308): Show | 317 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(314): Show |
intron_variant | MODIFIER | c.413+871G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59493260 | ||||||
| chr15:59493372
|
T | C | 1 | a0001c0002t0001g0022 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.413+983T>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59493372 | ||||||
| chr15:59493511
|
C | A | 19 | a0001c0002t0001g0056a0001c0002t0001g0135a0001c0002t0001g0136others(16): Show | 20 | HG01109.hp1 HG01516.hp2 HG01993.hp2 others(17): Show |
intron_variant | MODIFIER | c.413+1122C>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59493511 | ||||||
| chr15:59493551
|
T | C | 1 | a0001c0001t0001g0046 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.413+1162T>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59493551 | ||||||
| chr15:59493579
|
C | T | 1 | a0001c0001t0001g0219 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.413+1190C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59493579 | ||||||
| chr15:59493613
|
A | G | 2 | a0001c0002t0001g0350a0001c0002t0013g0239 | 2 | HG02615.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.413+1224A>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59493613 | ||||||
| chr15:59493692
|
A | C | 2 | a0001c0001t0001g0283a0001c0001t0001g0285 | 2 | NA18983.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.413+1303A>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59493692 | ||||||
| chr15:59493762
|
A | G | 1 | a0001c0001t0001g0105 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.413+1373A>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59493762 | ||||||
| chr15:59493782
|
T | A | 1 | a0001c0002t0012g0146 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.413+1393T>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59493782 | ||||||
| chr15:59493836
|
C | T | 15 | a0001c0002t0001g0011a0001c0002t0003g0139a0001c0002t0003g0141others(12): Show | 15 | HG01884.hp2 HG01891.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.413+1447C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59493836 | ||||||
| chr15:59493944
|
C | A | 3 | a0001c0002t0001g0135a0001c0002t0001g0136a0001c0002t0012g0146 | 3 | HG02895.hp1 HG02897.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.413+1555C>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59493944 | ||||||
| chr15:59493986
|
C | G | 1 | a0001c0002t0012g0146 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.413+1597C>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59493986 | ||||||
| chr15:59494059
|
A | G | 19 | a0001c0002t0001g0056a0001c0002t0001g0135a0001c0002t0001g0136others(16): Show | 20 | HG01109.hp1 HG01516.hp2 HG01993.hp2 others(17): Show |
intron_variant | MODIFIER | c.413+1670A>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59494059 | ||||||
| chr15:59494137
|
C | A | 25 | a0001c0002t0001g0056a0001c0002t0001g0135a0001c0002t0001g0136others(22): Show | 27 | HG01109.hp1 HG01516.hp2 HG01993.hp2 others(24): Show |
intron_variant | MODIFIER | c.413+1748C>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59494137 | ||||||
| chr15:59494174
|
A | G | 19 | a0001c0002t0001g0011a0001c0002t0003g0139a0001c0002t0003g0141others(16): Show | 19 | HG01884.hp2 HG01891.hp1 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.413+1785A>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59494174 | ||||||
| chr15:59494371
|
G | A | 19 | a0001c0002t0001g0056a0001c0002t0001g0135a0001c0002t0001g0136others(16): Show | 20 | HG01109.hp1 HG01516.hp2 HG01993.hp2 others(17): Show |
intron_variant | MODIFIER | c.413+1982G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59494371 | ||||||
| chr15:59494391
|
C | T | 2 | a0001c0002t0001g0350a0001c0002t0013g0239 | 2 | HG02615.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.413+2002C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59494391 | ||||||
| chr15:59494535
|
TC | T | 19 | a0001c0002t0001g0056a0001c0002t0001g0135a0001c0002t0001g0136others(16): Show | 20 | HG01109.hp1 HG01516.hp2 HG01993.hp2 others(17): Show |
intron_variant | MODIFIER | c.413+2147delC | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59494535 | ||||||
| chr15:59494550
|
A | AG | 19 | a0001c0002t0001g0056a0001c0002t0001g0135a0001c0002t0001g0136others(16): Show | 20 | HG01109.hp1 HG01516.hp2 HG01993.hp2 others(17): Show |
intron_variant | MODIFIER | c.413+2161_413+2162i others(3): Show |
FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59494550 | ||||||
| chr15:59494626
|
T | C | 25 | a0001c0002t0001g0056a0001c0002t0001g0135a0001c0002t0001g0136others(22): Show | 27 | HG01109.hp1 HG01516.hp2 HG01993.hp2 others(24): Show |
intron_variant | MODIFIER | c.413+2237T>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59494626 | ||||||
| chr15:59494761
|
A | G | 1 | a0001c0001t0001g0075 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.413+2372A>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59494761 | ||||||
| chr15:59494831
|
T | G | 44 | a0001c0002t0001g0011a0001c0002t0001g0056a0001c0002t0001g0135others(41): Show | 46 | HG01109.hp1 HG01516.hp2 HG01884.hp2 others(43): Show |
intron_variant | MODIFIER | c.413+2442T>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59494831 | ||||||
| chr15:59495154
|
A | C | 2 | a0001c0002t0001g0350a0001c0002t0013g0239 | 2 | HG02615.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.413+2765A>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59495154 | ||||||
| chr15:59495400
|
C | G | 1 | a0001c0001t0001g0070 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.413+3011C>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59495400 | ||||||
| chr15:59495413
|
T | C | 21 | a0001c0002t0001g0056a0001c0002t0001g0224a0001c0002t0001g0248others(18): Show | 23 | HG01109.hp1 HG01516.hp2 HG01993.hp2 others(20): Show |
intron_variant | MODIFIER | c.413+3024T>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59495413 | ||||||
| chr15:59495421
|
A | C | 20 | a0001c0002t0001g0056a0001c0002t0001g0248a0001c0002t0001g0330others(17): Show | 22 | HG01109.hp1 HG01516.hp2 HG01993.hp2 others(19): Show |
intron_variant | MODIFIER | c.413+3032A>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59495421 | ||||||
| chr15:59495616
|
C | T | 3 | a0001c0002t0001g0135a0001c0002t0001g0136a0001c0002t0012g0146 | 3 | HG02895.hp1 HG02897.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.413+3227C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59495616 | ||||||
| chr15:59495643
|
T | C | 3 | a0001c0002t0001g0135a0001c0002t0001g0136a0001c0002t0012g0146 | 3 | HG02895.hp1 HG02897.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.413+3254T>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59495643 | ||||||
| chr15:59495988
|
A | G | 26 | a0001c0001t0001g0144a0001c0002t0001g0056a0001c0002t0001g0135others(23): Show | 28 | HG01109.hp1 HG01516.hp2 HG01993.hp2 others(25): Show |
intron_variant | MODIFIER | c.413+3599A>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59495988 | ||||||
| chr15:59496037
|
A | G | 1 | a0001c0001t0001g0315 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.413+3648A>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59496037 | ||||||
| chr15:59496164
|
G | T | 239 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(236): Show | 244 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(241): Show |
intron_variant | MODIFIER | c.413+3775G>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59496164 | ||||||
| chr15:59496182
|
A | AT | 20 | a0001c0002t0001g0056a0001c0002t0001g0248a0001c0002t0001g0330others(17): Show | 22 | HG01109.hp1 HG01516.hp2 HG01993.hp2 others(19): Show |
intron_variant | MODIFIER | c.413+3800dupT | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr15 | 59496182 | |||||
| chr15:59496234
|
A | G | 1 | a0001c0001t0001g0283 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.413+3845A>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59496234 | ||||||
| chr15:59496276
|
C | A | 15 | a0001c0002t0001g0011a0001c0002t0003g0139a0001c0002t0003g0141others(12): Show | 15 | HG01884.hp2 HG01891.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.413+3887C>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59496276 | ||||||
| chr15:59496325
|
G | A | 1 | a0001c0001t0001g0151 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.413+3936G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59496325 | ||||||
| chr15:59496328
|
C | T | 5 | a0001c0001t0001g0243a0001c0001t0001g0249a0001c0001t0001g0250others(2): Show | 5 | NA18952.hp1 NA18957.hp2 NA18959.hp1 others(2): Show |
intron_variant | MODIFIER | c.413+3939C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59496328 | ||||||
| chr15:59496356
|
C | T | 2 | a0001c0002t0010g0257a0001c0002t0010g0258 | 2 | HG03098.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.413+3967C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59496356 | ||||||
| chr15:59496407
|
C | G | 6 | a0001c0002t0002g0050a0001c0002t0002g0145a0001c0003t0002g0004others(3): Show | 7 | HG02622.hp1 HG02630.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.413+4018C>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59496407 | ||||||
| chr15:59497128
|
A | AAAG | 9 | a0001c0001t0001g0032a0001c0001t0001g0055a0001c0001t0001g0133others(6): Show | 9 | HG01074.hp2 HG01256.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.413+4763_413+4765d others(5): Show |
FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr15 | 59497128 | |||||
| chr15:59497128
|
AAAG | A | 3 | a0001c0001t0001g0320a0001c0002t0001g0350a0001c0002t0013g0239 | 3 | HG02615.hp2 HG03453.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.413+4763_413+4765d others(5): Show |
FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr15 | 59497128 | |||||
| chr15:59497151
|
A | G | 1 | a0001c0002t0001g0330 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.413+4762A>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59497151 | ||||||
| chr15:59497179
|
G | A | 11 | a0001c0002t0001g0056a0001c0002t0001g0248a0001c0002t0004g0015others(8): Show | 12 | HG01109.hp1 HG01516.hp2 HG01993.hp2 others(9): Show |
intron_variant | MODIFIER | c.413+4790G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59497179 | ||||||
| chr15:59497185
|
C | T | 19 | a0001c0002t0001g0011a0001c0002t0003g0139a0001c0002t0003g0141others(16): Show | 19 | HG01884.hp2 HG01891.hp1 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.413+4796C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59497185 | ||||||
| chr15:59497229
|
C | T | 5 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0355others(2): Show | 5 | HG02818.hp2 HG02976.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.413+4840C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59497229 | ||||||
| chr15:59497402
|
T | C | 43 | a0001c0002t0001g0011a0001c0002t0001g0056a0001c0002t0001g0135others(40): Show | 45 | HG01109.hp1 HG01516.hp2 HG01884.hp2 others(42): Show |
intron_variant | MODIFIER | c.413+5013T>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59497402 | ||||||
| chr15:59497459
|
T | A | 2 | a0001c0002t0001g0350a0001c0002t0013g0239 | 2 | HG02615.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.413+5070T>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59497459 | ||||||
| chr15:59497516
|
G | A | 5 | a0001c0002t0001g0135a0001c0002t0001g0136a0001c0002t0001g0350others(2): Show | 5 | HG02615.hp2 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.413+5127G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59497516 | ||||||
| chr15:59497637
|
CTTGAGGC others(7): Show |
C | 20 | a0001c0001t0001g0234a0001c0002t0001g0011a0001c0002t0003g0139others(17): Show | 20 | HG01884.hp2 HG01891.hp1 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.413+5282_413+5295d others(16): Show |
FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr15 | 59497637 | |||||
| chr15:59497867
|
A | T | 1 | a0001c0001t0001g0334 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.413+5478A>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59497867 | ||||||
| chr15:59497911
|
G | T | 1 | a0001c0001t0001g0046 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.413+5522G>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59497911 | ||||||
| chr15:59497951
|
G | T | 1 | a0001c0002t0001g0053 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.413+5562G>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59497951 | ||||||
| chr15:59497981
|
T | C | 5 | a0001c0002t0001g0135a0001c0002t0001g0136a0001c0002t0001g0350others(2): Show | 5 | HG02615.hp2 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.413+5592T>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59497981 | ||||||
| chr15:59497982
|
G | A | 2 | a0001c0001t0001g0134a0001c0001t0001g0137 | 2 | HG02109.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.413+5593G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59497982 | ||||||
| chr15:59498091
|
C | CCTCT | 3 | a0001c0002t0001g0135a0001c0002t0001g0136a0001c0002t0012g0146 | 3 | HG02895.hp1 HG02897.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.413+5704_413+5707d others(6): Show |
FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr15 | 59498091 | |||||
| chr15:59498305
|
T | C | 15 | a0001c0002t0001g0011a0001c0002t0003g0139a0001c0002t0003g0141others(12): Show | 15 | HG01884.hp2 HG01891.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.413+5916T>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59498305 | ||||||
| chr15:59498353
|
T | C | 2 | a0001c0002t0001g0135a0001c0002t0001g0136 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.413+5964T>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59498353 | ||||||
| chr15:59498475
|
A | G | 1 | a0001c0002t0001g0330 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.413+6086A>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59498475 | ||||||
| chr15:59498677
|
A | G | 22 | a0001c0002t0001g0056a0001c0002t0001g0135a0001c0002t0001g0136others(19): Show | 24 | HG01109.hp1 HG01516.hp2 HG01993.hp2 others(21): Show |
intron_variant | MODIFIER | c.413+6288A>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59498677 | ||||||
| chr15:59498693
|
G | A | 5 | a0001c0001t0001g0046a0001c0001t0001g0178a0001c0001t0001g0179others(2): Show | 5 | HG00733.hp1 HG01168.hp2 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.413+6304G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59498693 | ||||||
| chr15:59498780
|
G | A | 3 | a0001c0001t0001g0355a0001c0001t0001g0357a0001c0001t0001g0358 | 3 | HG02818.hp2 HG06807.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.413+6391G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59498780 | ||||||
| chr15:59498804
|
G | A | 1 | a0001c0002t0003g0225 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.413+6415G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59498804 | ||||||
| chr15:59498842
|
A | T | 1 | a0001c0001t0001g0305 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.413+6453A>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59498842 | ||||||
| chr15:59498875
|
G | A | 1 | a0001c0002t0001g0350 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.413+6486G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59498875 | ||||||
| chr15:59498888
|
C | G | 1 | a0001c0001t0001g0288 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.413+6499C>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59498888 | ||||||
| chr15:59498959
|
G | A | 2 | a0001c0002t0001g0350a0001c0002t0013g0239 | 2 | HG02615.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.413+6570G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59498959 | ||||||
| chr15:59499013
|
G | C | 4 | a0001c0002t0005g0273a0001c0002t0005g0274a0001c0002t0005g0275others(1): Show | 4 | HG02559.hp2 HG02723.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.413+6624G>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59499013 | ||||||
| chr15:59499121
|
A | T | 249 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(246): Show | 254 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(251): Show |
intron_variant | MODIFIER | c.413+6732A>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59499121 | ||||||
| chr15:59499391
|
A | G | 6 | a0001c0002t0002g0050a0001c0002t0002g0145a0001c0003t0002g0004others(3): Show | 7 | HG02622.hp1 HG02630.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.413+7002A>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59499391 | ||||||
| chr15:59499431
|
A | G | 1 | a0001c0001t0001g0193 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.413+7042A>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59499431 | ||||||
| chr15:59499467
|
C | T | 1 | a0001c0001t0001g0288 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.413+7078C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59499467 | ||||||
| chr15:59499531
|
A | T | 363 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(360): Show | 373 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(370): Show |
intron_variant | MODIFIER | c.413+7142A>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59499531 | ||||||
| chr15:59499661
|
AGTAAGAT others(12): Show |
A | 1 | a0001c0001t0001g0295 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.413+7289_413+7307d others(21): Show |
FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr15 | 59499661 | |||||
| chr15:59499859
|
A | AT | 36 | a0001c0001t0001g0113a0001c0001t0001g0157a0001c0001t0001g0173others(33): Show | 36 | HG01081.hp1 HG01361.hp1 HG01884.hp2 others(33): Show |
intron_variant | MODIFIER | c.414-7339dupT | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr15 | 59499859 | |||||
| chr15:59499859
|
A | ATT | 9 | a0001c0002t0001g0056a0001c0002t0004g0015a0001c0002t0004g0244others(6): Show | 10 | HG01109.hp1 HG01516.hp2 HG01993.hp2 others(7): Show |
intron_variant | MODIFIER | c.414-7340_414-7339d others(4): Show |
FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr15 | 59499859 | |||||
| chr15:59499886
|
C | G | 1 | a0001c0001t0001g0290 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.414-7327C>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59499886 | ||||||
| chr15:59499958
|
G | A | 3 | a0001c0002t0003g0225a0001c0002t0003g0228a0001c0002t0015g0227 | 3 | HG02486.hp1 HG02922.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.414-7255G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59499958 | ||||||
| chr15:59500099
|
C | T | 1 | a0001c0002t0001g0350 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.414-7114C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59500099 | ||||||
| chr15:59500173
|
C | T | 1 | a0001c0001t0001g0075 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.414-7040C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59500173 | ||||||
| chr15:59500410
|
A | C | 1 | a0001c0001t0001g0322 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.414-6803A>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59500410 | ||||||
| chr15:59500465
|
G | A | 2 | a0001c0001t0001g0269a0001c0001t0001g0287 | 2 | NA18989.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.414-6748G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59500465 | ||||||
| chr15:59500759
|
C | G | 15 | a0001c0002t0001g0011a0001c0002t0003g0139a0001c0002t0003g0141others(12): Show | 15 | HG01884.hp2 HG01891.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.414-6454C>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59500759 | ||||||
| chr15:59500803
|
T | A | 5 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0054others(2): Show | 7 | HG01081.hp2 HG01168.hp1 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.414-6410T>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59500803 | ||||||
| chr15:59501000
|
A | G | 9 | a0001c0002t0001g0135a0001c0002t0001g0136a0001c0002t0002g0050others(6): Show | 10 | HG02622.hp1 HG02630.hp1 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.414-6213A>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59501000 | ||||||
| chr15:59501235
|
T | C | 1 | a0001c0002t0001g0029 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.414-5978T>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59501235 | ||||||
| chr15:59501408
|
G | A | 8 | a0001c0002t0001g0056a0001c0002t0004g0244a0001c0002t0004g0246others(5): Show | 8 | HG01109.hp1 HG01516.hp2 HG01993.hp2 others(5): Show |
intron_variant | MODIFIER | c.414-5805G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59501408 | ||||||
| chr15:59501410
|
C | T | 15 | a0001c0002t0001g0011a0001c0002t0003g0139a0001c0002t0003g0141others(12): Show | 15 | HG01884.hp2 HG01891.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.414-5803C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59501410 | ||||||
| chr15:59501413
|
A | G | 1 | a0001c0001t0001g0094 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.414-5800A>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59501413 | ||||||
| chr15:59501572
|
A | G | 1 | a0001c0001t0001g0097 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.414-5641A>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59501572 | ||||||
| chr15:59501935
|
C | G | 1 | a0001c0002t0006g0028 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.414-5278C>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59501935 | ||||||
| chr15:59502148
|
T | G | 2 | a0001c0002t0001g0135a0001c0002t0001g0136 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.414-5065T>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59502148 | ||||||
| chr15:59502243
|
A | T | 1 | a0001c0002t0014g0140 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.414-4970A>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59502243 | ||||||
| chr15:59502327
|
T | C | 22 | a0001c0002t0001g0056a0001c0002t0001g0135a0001c0002t0001g0136others(19): Show | 24 | HG01109.hp1 HG01516.hp2 HG01993.hp2 others(21): Show |
intron_variant | MODIFIER | c.414-4886T>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59502327 | ||||||
| chr15:59502331
|
G | A | 1 | a0001c0002t0004g0015 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.414-4882G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59502331 | ||||||
| chr15:59502339
|
C | G | 1 | a0001c0001t0001g0226 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.414-4874C>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59502339 | ||||||
| chr15:59502340
|
C | A | 1 | a0001c0002t0006g0028 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.414-4873C>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59502340 | ||||||
| chr15:59502341
|
C | CA | 7 | a0001c0001t0001g0230a0001c0001t0001g0231a0001c0001t0001g0232others(4): Show | 7 | HG01109.hp2 HG01243.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.414-4870dupA | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr15 | 59502341 | |||||
| chr15:59502485
|
C | CTG | 100 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(97): Show | 105 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.414-4686_414-4685d others(4): Show |
FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr15 | 59502485 | |||||
| chr15:59502485
|
C | CTGTG | 77 | a0001c0001t0001g0030a0001c0001t0001g0057a0001c0001t0001g0063others(74): Show | 78 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(75): Show |
intron_variant | MODIFIER | c.414-4688_414-4685d others(6): Show |
FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr15 | 59502485 | |||||
| chr15:59502485
|
C | CTGTGTG | 34 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0068others(31): Show | 35 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(32): Show |
intron_variant | MODIFIER | c.414-4690_414-4685d others(8): Show |
FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr15 | 59502485 | |||||
| chr15:59502485
|
C | CTGTGTGT others(1): Show |
11 | a0001c0001t0001g0098a0001c0001t0001g0129a0001c0001t0001g0131others(8): Show | 11 | HG01109.hp1 HG02109.hp2 HG02155.hp2 others(8): Show |
intron_variant | MODIFIER | c.414-4692_414-4685d others(10): Show |
FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr15 | 59502485 | |||||
| chr15:59502485
|
C | CTGTGTGT others(3): Show |
3 | a0001c0001t0001g0312a0001c0002t0001g0035a0001c0002t0001g0036 | 3 | HG01515.hp2 HG01517.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.414-4694_414-4685d others(12): Show |
FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr15 | 59502485 | |||||
| chr15:59502485
|
CTG | C | 26 | a0001c0001t0001g0046a0001c0001t0001g0087a0001c0001t0001g0096others(23): Show | 27 | HG00733.hp1 HG01109.hp2 HG01168.hp2 others(24): Show |
intron_variant | MODIFIER | c.414-4686_414-4685d others(4): Show |
FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr15 | 59502485 | |||||
| chr15:59502485
|
CTGTG | C | 12 | a0001c0001t0001g0077a0001c0001t0001g0158a0001c0001t0001g0159others(9): Show | 12 | HG01081.hp1 HG01243.hp1 HG02155.hp1 others(9): Show |
intron_variant | MODIFIER | c.414-4688_414-4685d others(6): Show |
FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr15 | 59502485 | |||||
| chr15:59502485
|
CTGTGTG | C | 5 | a0001c0001t0001g0149a0001c0001t0001g0160a0001c0001t0001g0164others(2): Show | 5 | HG01256.hp1 HG01361.hp1 HG02132.hp1 others(2): Show |
intron_variant | MODIFIER | c.414-4690_414-4685d others(8): Show |
FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr15 | 59502485 | |||||
| chr15:59502523
|
G | C | 3 | a0001c0001t0001g0160a0001c0001t0001g0164a0001c0001t0001g0360 | 3 | HG02132.hp1 NA18957.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.414-4690G>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59502523 | ||||||
| chr15:59502529
|
T | G | 1 | a0001c0001t0001g0338 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.414-4684T>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59502529 | ||||||
| chr15:59502557
|
A | C | 1 | a0001c0001t0001g0348 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.414-4656A>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59502557 | ||||||
| chr15:59502583
|
G | A | 1 | a0001c0002t0001g0041 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.414-4630G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59502583 | ||||||
| chr15:59502658
|
C | T | 2 | a0001c0002t0001g0035a0001c0002t0001g0036 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.414-4555C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59502658 | ||||||
| chr15:59502674
|
C | T | 1 | a0001c0001t0001g0344 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.414-4539C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59502674 | ||||||
| chr15:59502692
|
T | C | 3 | a0001c0002t0001g0135a0001c0002t0001g0136a0001c0002t0012g0146 | 3 | HG02895.hp1 HG02897.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.414-4521T>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59502692 | ||||||
| chr15:59502773
|
C | T | 15 | a0001c0002t0001g0011a0001c0002t0003g0139a0001c0002t0003g0141others(12): Show | 15 | HG01884.hp2 HG01891.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.414-4440C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59502773 | ||||||
| chr15:59502811
|
G | A | 2 | a0001c0002t0001g0350a0001c0002t0013g0239 | 2 | HG02615.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.414-4402G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59502811 | ||||||
| chr15:59502816
|
A | G | 258 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(255): Show | 265 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(262): Show |
intron_variant | MODIFIER | c.414-4397A>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59502816 | ||||||
| chr15:59502907
|
A | C | 1 | a0001c0001t0001g0284 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.414-4306A>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59502907 | ||||||
| chr15:59503111
|
G | A | 2 | a0001c0002t0004g0015a0001c0002t0011g0010 | 3 | HG02647.hp1 HG02970.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.414-4102G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59503111 | ||||||
| chr15:59503233
|
C | CA | 60 | a0001c0001t0001g0019a0001c0001t0001g0058a0001c0001t0001g0063others(57): Show | 60 | HG00544.hp2 HG00642.hp1 HG00741.hp2 others(57): Show |
intron_variant | MODIFIER | c.414-3956dupA | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr15 | 59503233 | |||||
| chr15:59503233
|
CA | C | 10 | a0001c0001t0001g0046a0001c0001t0001g0092a0001c0001t0001g0095others(7): Show | 10 | HG01069.hp1 HG01099.hp2 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.414-3956delA | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr15 | 59503233 | |||||
| chr15:59503320
|
C | T | 1 | a0001c0001t0001g0226 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.414-3893C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59503320 | ||||||
| chr15:59503370
|
TA | T | 250 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(247): Show | 255 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(252): Show |
intron_variant | MODIFIER | c.414-3842delA | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59503370 | ||||||
| chr15:59503459
|
A | G | 3 | a0001c0002t0001g0135a0001c0002t0001g0136a0001c0002t0012g0146 | 3 | HG02895.hp1 HG02897.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.414-3754A>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59503459 | ||||||
| chr15:59503565
|
A | G | 2 | a0001c0002t0001g0350a0001c0002t0013g0239 | 2 | HG02615.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.414-3648A>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59503565 | ||||||
| chr15:59503579
|
T | TG | 9 | a0001c0002t0001g0135a0001c0002t0001g0136a0001c0002t0002g0050others(6): Show | 10 | HG02622.hp1 HG02630.hp1 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.414-3634_414-3633i others(3): Show |
FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59503579 | ||||||
| chr15:59503580
|
A | AT | 13 | a0001c0001t0001g0129a0001c0002t0001g0056a0001c0002t0004g0015others(10): Show | 14 | HG01109.hp1 HG01516.hp2 HG01993.hp2 others(11): Show |
intron_variant | MODIFIER | c.414-3621dupT | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr15 | 59503580 | |||||
| chr15:59503580
|
A | T | 9 | a0001c0002t0001g0135a0001c0002t0001g0136a0001c0002t0002g0050others(6): Show | 10 | HG02622.hp1 HG02630.hp1 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.414-3633A>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59503580 | ||||||
| chr15:59503770
|
C | G | 363 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(360): Show | 373 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(370): Show |
intron_variant | MODIFIER | c.414-3443C>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59503770 | ||||||
| chr15:59503802
|
G | C | 2 | a0001c0002t0001g0350a0001c0002t0013g0239 | 2 | HG02615.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.414-3411G>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59503802 | ||||||
| chr15:59503870
|
G | A | 1 | a0001c0001t0001g0075 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.414-3343G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59503870 | ||||||
| chr15:59503871
|
C | T | 1 | a0001c0001t0001g0131 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.414-3342C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59503871 | ||||||
| chr15:59503880
|
C | T | 1 | a0001c0001t0001g0219 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.414-3333C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59503880 | ||||||
| chr15:59504016
|
C | T | 1 | a0001c0002t0001g0248 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.414-3197C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59504016 | ||||||
| chr15:59504325
|
C | G | 1 | a0001c0001t0001g0162 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.414-2888C>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59504325 | ||||||
| chr15:59504354
|
C | T | 1 | a0001c0001t0001g0182 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.414-2859C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59504354 | ||||||
| chr15:59504707
|
A | AAC | 15 | a0001c0002t0001g0056a0001c0002t0001g0135a0001c0002t0001g0136others(12): Show | 16 | HG01109.hp1 HG01516.hp2 HG01993.hp2 others(13): Show |
intron_variant | MODIFIER | c.414-2505_414-2504i others(4): Show |
FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr15 | 59504707 | |||||
| chr15:59504882
|
T | C | 2 | a0001c0002t0004g0015a0001c0002t0011g0010 | 3 | HG02647.hp1 HG02970.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.414-2331T>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59504882 | ||||||
| chr15:59504920
|
C | T | 2 | a0001c0001t0001g0336a0001c0001t0001g0338 | 2 | HG02055.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.414-2293C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59504920 | ||||||
| chr15:59504955
|
G | T | 135 | a0001c0001t0001g0063a0001c0001t0001g0091a0001c0001t0001g0092others(132): Show | 137 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(134): Show |
intron_variant | MODIFIER | c.414-2258G>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59504955 | ||||||
| chr15:59504990
|
A | G | 37 | a0001c0002t0001g0011a0001c0002t0001g0056a0001c0002t0001g0135others(34): Show | 39 | HG01109.hp1 HG01516.hp2 HG01884.hp2 others(36): Show |
intron_variant | MODIFIER | c.414-2223A>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59504990 | ||||||
| chr15:59505033
|
T | C | 1 | a0001c0002t0001g0011 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.414-2180T>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59505033 | ||||||
| chr15:59505094
|
A | G | 1 | a0001c0001t0001g0083 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.414-2119A>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59505094 | ||||||
| chr15:59505165
|
C | T | 2 | a0001c0002t0010g0257a0001c0002t0010g0258 | 2 | HG03098.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.414-2048C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59505165 | ||||||
| chr15:59505229
|
G | A | 10 | a0001c0002t0001g0056a0001c0002t0004g0015a0001c0002t0004g0244others(7): Show | 11 | HG01109.hp1 HG01516.hp2 HG01993.hp2 others(8): Show |
intron_variant | MODIFIER | c.414-1984G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59505229 | ||||||
| chr15:59505282
|
C | T | 107 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(104): Show | 110 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(107): Show |
intron_variant | MODIFIER | c.414-1931C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59505282 | ||||||
| chr15:59505358
|
A | G | 6 | a0001c0002t0002g0050a0001c0002t0002g0145a0001c0003t0002g0004others(3): Show | 7 | HG02622.hp1 HG02630.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.414-1855A>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59505358 | ||||||
| chr15:59505460
|
C | T | 1 | a0001c0002t0003g0271 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.414-1753C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59505460 | ||||||
| chr15:59505511
|
C | T | 13 | a0001c0001t0001g0027a0001c0001t0001g0154a0001c0001t0001g0181others(10): Show | 13 | HG00738.hp1 HG02015.hp1 HG02027.hp2 others(10): Show |
intron_variant | MODIFIER | c.414-1702C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59505511 | ||||||
| chr15:59505512
|
G | A | 15 | a0001c0002t0001g0011a0001c0002t0003g0139a0001c0002t0003g0141others(12): Show | 15 | HG01884.hp2 HG01891.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.414-1701G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59505512 | ||||||
| chr15:59505512
|
G | GA | 19 | a0001c0001t0001g0077a0001c0002t0001g0056a0001c0002t0001g0135others(16): Show | 21 | HG01109.hp1 HG01516.hp2 HG01993.hp2 others(18): Show |
intron_variant | MODIFIER | c.414-1686dupA | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr15 | 59505512 | |||||
| chr15:59505553
|
T | C | 6 | a0001c0001t0001g0231a0001c0001t0001g0232a0001c0001t0001g0233others(3): Show | 6 | HG01243.hp2 HG02145.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.414-1660T>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59505553 | ||||||
| chr15:59505605
|
A | G | 1 | a0001c0001t0019g0223 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.414-1608A>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59505605 | ||||||
| chr15:59505841
|
T | A | 1 | a0001c0001t0001g0187 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.414-1372T>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59505841 | ||||||
| chr15:59506133
|
A | G | 1 | a0001c0001t0001g0303 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.414-1080A>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59506133 | ||||||
| chr15:59506154
|
G | GT | 11 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0016others(8): Show | 13 | HG00735.hp1 HG00741.hp2 HG01074.hp2 others(10): Show |
intron_variant | MODIFIER | c.414-1056dupT | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr15 | 59506154 | |||||
| chr15:59506320
|
T | C | 5 | a0001c0002t0001g0007a0001c0002t0001g0012a0001c0002t0001g0013others(2): Show | 6 | NA18955.hp2 NA18981.hp2 NA18985.hp2 others(3): Show |
intron_variant | MODIFIER | c.414-893T>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59506320 | ||||||
| chr15:59506410
|
A | G | 1 | a0001c0001t0001g0322 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.414-803A>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59506410 | ||||||
| chr15:59506431
|
G | T | 15 | a0001c0002t0001g0011a0001c0002t0003g0139a0001c0002t0003g0141others(12): Show | 15 | HG01884.hp2 HG01891.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.414-782G>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59506431 | ||||||
| chr15:59506472
|
G | A | 6 | a0001c0001t0001g0231a0001c0001t0001g0232a0001c0001t0001g0233others(3): Show | 6 | HG01243.hp2 HG02145.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.414-741G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59506472 | ||||||
| chr15:59506576
|
C | A | 6 | a0001c0002t0002g0050a0001c0002t0002g0145a0001c0003t0002g0004others(3): Show | 7 | HG02622.hp1 HG02630.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.414-637C>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59506576 | ||||||
| chr15:59506617
|
C | T | 12 | a0001c0001t0001g0265a0001c0001t0001g0266a0001c0001t0001g0267others(9): Show | 12 | HG01069.hp2 HG01071.hp1 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.414-596C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59506617 | ||||||
| chr15:59506673
|
G | A | 1 | a0001c0001t0009g0167 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.414-540G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59506673 | ||||||
| chr15:59506740
|
G | A | 1 | a0001c0001t0001g0262 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.414-473G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59506740 | ||||||
| chr15:59506839
|
T | G | 37 | a0001c0001t0001g0144a0001c0002t0001g0011a0001c0002t0001g0056others(34): Show | 39 | HG01109.hp1 HG01516.hp2 HG01884.hp2 others(36): Show |
intron_variant | MODIFIER | c.414-374T>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59506839 | ||||||
| chr15:59506943
|
C | T | 2 | a0001c0001t0001g0159a0001c0001t0009g0167 | 2 | HG01243.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.414-270C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59506943 | ||||||
| chr15:59507076
|
A | C | 1 | a0001c0001t0001g0144 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.414-137A>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59507076 | ||||||
| chr15:59507079
|
T | C | 262 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(259): Show | 269 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(266): Show |
intron_variant | MODIFIER | c.414-134T>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59507079 | ||||||
| chr15:59507132
|
G | A | 13 | a0001c0001t0001g0027a0001c0001t0001g0154a0001c0001t0001g0181others(10): Show | 13 | HG00738.hp1 HG02015.hp1 HG02027.hp2 others(10): Show |
intron_variant | MODIFIER | c.414-81G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59507132 | ||||||
| chr15:59507155
|
C | G | 9 | a0001c0001t0001g0063a0001c0001t0001g0091a0001c0001t0001g0092others(6): Show | 9 | HG01069.hp1 HG01071.hp2 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.414-58C>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 4/8 | chr15 | 59507155 | ||||||
| chr15:59507444
|
C | G | 14 | a0001c0001t0001g0016a0001c0001t0001g0147a0001c0001t0001g0265others(11): Show | 14 | HG01069.hp2 HG01071.hp1 HG01099.hp1 others(11): Show |
intron_variant | MODIFIER | c.543+102C>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 5/8 | chr15 | 59507444 | ||||||
| chr15:59507451
|
G | T | 1 | a0001c0001t0001g0045 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.543+109G>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 5/8 | chr15 | 59507451 | ||||||
| chr15:59507459
|
G | A | 2 | a0001c0001t0001g0345a0001c0001t0001g0346 | 2 | HG00423.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.543+117G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 5/8 | chr15 | 59507459 | ||||||
| chr15:59507679
|
C | G | 1 | a0001c0001t0001g0162 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.543+337C>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 5/8 | chr15 | 59507679 | ||||||
| chr15:59507839
|
T | G | 1 | a0001c0001t0001g0342 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.543+497T>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 5/8 | chr15 | 59507839 | ||||||
| chr15:59508422
|
T | C | 1 | a0001c0001t0001g0095 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.544-441T>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 5/8 | chr15 | 59508422 | ||||||
| chr15:59508526
|
T | G | 6 | a0001c0002t0002g0050a0001c0002t0002g0145a0001c0003t0002g0004others(3): Show | 7 | HG02622.hp1 HG02630.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.544-337T>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 5/8 | chr15 | 59508526 | ||||||
| chr15:59508585
|
C | G | 13 | a0001c0001t0001g0077a0001c0001t0001g0149a0001c0001t0001g0158others(10): Show | 13 | HG01243.hp1 HG01256.hp1 HG02132.hp1 others(10): Show |
intron_variant | MODIFIER | c.544-278C>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 5/8 | chr15 | 59508585 | ||||||
| chr15:59508789
|
G | C | 1 | a0001c0001t0001g0342 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.544-74G>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 5/8 | chr15 | 59508789 | ||||||
| chr15:59508790
|
C | T | 1 | a0001c0001t0001g0342 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.544-73C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 5/8 | chr15 | 59508790 | ||||||
| chr15:59509043
|
C | G | 2 | a0001c0001t0001g0114a0001c0001t0001g0115 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.650+74C>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 6/8 | chr15 | 59509043 | ||||||
| chr15:59509101
|
T | G | 1 | a0001c0001t0001g0342 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.650+132T>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 6/8 | chr15 | 59509101 | ||||||
| chr15:59509194
|
G | A | 5 | a0001c0001t0001g0148a0001c0001t0001g0183a0001c0001t0001g0294others(2): Show | 5 | NA18967.hp2 NA18970.hp2 NA18981.hp1 others(2): Show |
intron_variant | MODIFIER | c.650+225G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 6/8 | chr15 | 59509194 | ||||||
| chr15:59509226
|
T | G | 2 | a0001c0001t0001g0144a0001c0002t0001g0011 | 2 | HG01891.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.650+257T>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 6/8 | chr15 | 59509226 | ||||||
| chr15:59509423
|
C | T | 6 | a0001c0002t0002g0050a0001c0002t0002g0145a0001c0003t0002g0004others(3): Show | 7 | HG02622.hp1 HG02630.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.650+454C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 6/8 | chr15 | 59509423 | ||||||
| chr15:59509523
|
A | G | 1 | a0001c0001t0001g0327 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.650+554A>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 6/8 | chr15 | 59509523 | ||||||
| chr15:59509614
|
G | A | 1 | a0001c0001t0001g0305 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.650+645G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 6/8 | chr15 | 59509614 | ||||||
| chr15:59509828
|
C | G | 5 | a0001c0001t0001g0160a0001c0001t0001g0162a0001c0001t0001g0164others(2): Show | 5 | HG02132.hp1 NA18957.hp1 NA18960.hp2 others(2): Show |
intron_variant | MODIFIER | c.650+859C>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 6/8 | chr15 | 59509828 | ||||||
| chr15:59509953
|
A | G | 14 | a0001c0002t0003g0139a0001c0002t0003g0141a0001c0002t0003g0142others(11): Show | 14 | HG01884.hp2 HG02451.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.650+984A>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 6/8 | chr15 | 59509953 | ||||||
| chr15:59510018
|
A | G | 2 | a0001c0001t0001g0193a0001c0001t0001g0206 | 2 | NA18982.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.650+1049A>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 6/8 | chr15 | 59510018 | ||||||
| chr15:59510044
|
T | C | 1 | a0001c0002t0001g0042 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.650+1075T>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 6/8 | chr15 | 59510044 | ||||||
| chr15:59510097
|
G | A | 4 | a0001c0001t0001g0148a0001c0001t0001g0294a0001c0001t0001g0312others(1): Show | 4 | NA18967.hp2 NA18970.hp2 NA18981.hp1 others(1): Show |
intron_variant | MODIFIER | c.650+1128G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 6/8 | chr15 | 59510097 | ||||||
| chr15:59510281
|
G | C | 4 | a0001c0003t0002g0004a0001c0003t0002g0051a0001c0003t0002g0052others(1): Show | 5 | HG02622.hp1 HG02630.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.650+1312G>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 6/8 | chr15 | 59510281 | ||||||
| chr15:59510347
|
C | A | 1 | a0001c0002t0003g0141 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.650+1378C>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 6/8 | chr15 | 59510347 | ||||||
| chr15:59510368
|
C | CA | 30 | a0001c0001t0001g0144a0001c0001t0001g0150a0001c0001t0001g0161others(27): Show | 32 | HG01109.hp1 HG01516.hp2 HG01993.hp2 others(29): Show |
intron_variant | MODIFIER | c.650+1414dupA | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr15 | 59510368 | |||||
| chr15:59510368
|
C | CAA | 15 | a0001c0002t0001g0011a0001c0002t0003g0139a0001c0002t0003g0141others(12): Show | 15 | HG01884.hp2 HG01891.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.650+1413_650+1414d others(4): Show |
FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr15 | 59510368 | |||||
| chr15:59510368
|
CA | C | 50 | a0001c0001t0001g0009a0001c0001t0001g0019a0001c0001t0001g0077others(47): Show | 51 | HG00609.hp2 HG00738.hp1 HG01243.hp1 others(48): Show |
intron_variant | MODIFIER | c.650+1414delA | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr15 | 59510368 | |||||
| chr15:59510409
|
T | A | 99 | a0001c0001t0001g0016a0001c0001t0001g0063a0001c0001t0001g0083others(96): Show | 99 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.650+1440T>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 6/8 | chr15 | 59510409 | ||||||
| chr15:59510475
|
T | C | 6 | a0001c0001t0001g0009a0001c0001t0001g0189a0001c0001t0001g0194others(3): Show | 7 | HG01346.hp2 HG01928.hp2 HG01952.hp1 others(4): Show |
intron_variant | MODIFIER | c.650+1506T>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 6/8 | chr15 | 59510475 | ||||||
| chr15:59510655
|
A | C | 6 | a0001c0002t0002g0050a0001c0002t0002g0145a0001c0003t0002g0004others(3): Show | 7 | HG02622.hp1 HG02630.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.650+1686A>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 6/8 | chr15 | 59510655 | ||||||
| chr15:59510655
|
A | G | 1 | a0001c0001t0001g0071 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.650+1686A>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 6/8 | chr15 | 59510655 | ||||||
| chr15:59510731
|
T | C | 1 | a0001c0002t0001g0029 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.650+1762T>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 6/8 | chr15 | 59510731 | ||||||
| chr15:59510777
|
C | CA | 93 | a0001c0001t0001g0057a0001c0001t0001g0063a0001c0001t0001g0083others(90): Show | 94 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.650+1838dupA | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr15 | 59510777 | |||||
| chr15:59510777
|
C | CAA | 32 | a0001c0001t0001g0147a0001c0001t0001g0148a0001c0001t0001g0157others(29): Show | 32 | HG00423.hp2 HG01891.hp1 HG02055.hp1 others(29): Show |
intron_variant | MODIFIER | c.650+1837_650+1838d others(4): Show |
FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr15 | 59510777 | |||||
| chr15:59510777
|
C | CAAA | 13 | a0001c0001t0001g0144a0001c0001t0001g0190a0001c0001t0001g0240others(10): Show | 13 | HG02451.hp2 HG02809.hp2 HG02895.hp1 others(10): Show |
intron_variant | MODIFIER | c.650+1836_650+1838d others(5): Show |
FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr15 | 59510777 | |||||
| chr15:59510777
|
C | CAAAA | 8 | a0001c0001t0019g0223a0001c0002t0003g0142a0001c0002t0003g0143others(5): Show | 8 | HG01884.hp2 HG02486.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.650+1835_650+1838d others(6): Show |
FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr15 | 59510777 | |||||
| chr15:59510777
|
CA | C | 93 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0025others(90): Show | 96 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.650+1838delA | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr15 | 59510777 | |||||
| chr15:59510777
|
CAA | C | 6 | a0001c0001t0001g0046a0001c0001t0001g0066a0001c0001t0001g0068others(3): Show | 6 | HG00558.hp1 HG01168.hp2 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.650+1837_650+1838d others(4): Show |
FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr15 | 59510777 | |||||
| chr15:59510777
|
CAAAAAAA others(3): Show |
C | 5 | a0001c0002t0005g0236a0001c0002t0005g0273a0001c0002t0005g0274others(2): Show | 5 | HG02258.hp1 HG02559.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.650+1829_650+1838d others(12): Show |
FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr15 | 59510777 | |||||
| chr15:59510777
|
CAAAAAAA others(4): Show |
C | 2 | a0001c0002t0001g0056a0001c0002t0004g0247 | 2 | HG01993.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.650+1828_650+1838d others(13): Show |
FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr15 | 59510777 | |||||
| chr15:59510777
|
CAAAAAAA others(11): Show |
C | 1 | a0001c0002t0012g0146 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.650+1821_650+1838d others(20): Show |
FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr15 | 59510777 | |||||
| chr15:59510879
|
G | A | 3 | a0001c0001t0001g0169a0001c0001t0001g0182a0001c0001t0001g0356 | 3 | HG02895.hp2 HG03041.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.650+1910G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 6/8 | chr15 | 59510879 | ||||||
| chr15:59511090
|
C | T | 1 | a0001c0001t0001g0181 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.650+2121C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 6/8 | chr15 | 59511090 | ||||||
| chr15:59511108
|
C | T | 2 | a0001c0001t0001g0144a0001c0002t0001g0011 | 2 | HG01891.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.650+2139C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 6/8 | chr15 | 59511108 | ||||||
| chr15:59511224
|
G | T | 1 | a0001c0001t0001g0199 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.650+2255G>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 6/8 | chr15 | 59511224 | ||||||
| chr15:59511265
|
GACA | G | 8 | a0001c0002t0001g0056a0001c0002t0004g0244a0001c0002t0004g0246others(5): Show | 8 | HG01109.hp1 HG01516.hp2 HG01993.hp2 others(5): Show |
intron_variant | MODIFIER | c.650+2300_650+2302d others(5): Show |
FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr15 | 59511265 | |||||
| chr15:59511443
|
G | A | 2 | a0001c0001t0001g0098a0001c0001t0001g0348 | 2 | HG02683.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.650+2474G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 6/8 | chr15 | 59511443 | ||||||
| chr15:59511473
|
C | G | 1 | a0004c0008t0001g0309 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.650+2504C>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 6/8 | chr15 | 59511473 | ||||||
| chr15:59511547
|
T | A | 21 | a0001c0002t0001g0056a0001c0002t0001g0135a0001c0002t0001g0136others(18): Show | 23 | HG01109.hp1 HG01516.hp2 HG01993.hp2 others(20): Show |
intron_variant | MODIFIER | c.650+2578T>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 6/8 | chr15 | 59511547 | ||||||
| chr15:59511585
|
T | G | 1 | a0001c0001t0001g0263 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.650+2616T>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 6/8 | chr15 | 59511585 | ||||||
| chr15:59511593
|
T | G | 5 | a0001c0002t0005g0236a0001c0002t0005g0273a0001c0002t0005g0274others(2): Show | 5 | HG02258.hp1 HG02559.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.650+2624T>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 6/8 | chr15 | 59511593 | ||||||
| chr15:59511851
|
A | G | 6 | a0001c0002t0002g0050a0001c0002t0002g0145a0001c0003t0002g0004others(3): Show | 7 | HG02622.hp1 HG02630.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.651-2438A>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 6/8 | chr15 | 59511851 | ||||||
| chr15:59511863
|
A | G | 1 | a0001c0001t0001g0284 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.651-2426A>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 6/8 | chr15 | 59511863 | ||||||
| chr15:59512216
|
C | T | 1 | a0001c0001t0001g0317 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.651-2073C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 6/8 | chr15 | 59512216 | ||||||
| chr15:59512306
|
G | C | 363 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(360): Show | 373 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(370): Show |
intron_variant | MODIFIER | c.651-1983G>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 6/8 | chr15 | 59512306 | ||||||
| chr15:59512345
|
G | A | 1 | a0001c0001t0001g0348 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.651-1944G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 6/8 | chr15 | 59512345 | ||||||
| chr15:59512379
|
G | A | 102 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(99): Show | 105 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.651-1910G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 6/8 | chr15 | 59512379 | ||||||
| chr15:59512434
|
T | C | 1 | a0001c0001t0001g0188 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.651-1855T>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 6/8 | chr15 | 59512434 | ||||||
| chr15:59512471
|
C | CA | 55 | a0001c0001t0001g0061a0001c0001t0001g0063a0001c0001t0001g0064others(52): Show | 57 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.651-1792dupA | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr15 | 59512471 | |||||
| chr15:59512471
|
CA | C | 29 | a0001c0001t0001g0057a0001c0001t0001g0116a0001c0001t0001g0144others(26): Show | 29 | HG01884.hp2 HG01891.hp1 HG02015.hp1 others(26): Show |
intron_variant | MODIFIER | c.651-1792delA | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr15 | 59512471 | |||||
| chr15:59512601
|
C | T | 8 | a0001c0002t0001g0056a0001c0002t0004g0244a0001c0002t0004g0246others(5): Show | 8 | HG01109.hp1 HG01516.hp2 HG01993.hp2 others(5): Show |
intron_variant | MODIFIER | c.651-1688C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 6/8 | chr15 | 59512601 | ||||||
| chr15:59512612
|
C | T | 6 | a0001c0002t0002g0050a0001c0002t0002g0145a0001c0003t0002g0004others(3): Show | 7 | HG02622.hp1 HG02630.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.651-1677C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 6/8 | chr15 | 59512612 | ||||||
| chr15:59512883
|
G | T | 15 | a0001c0002t0001g0056a0001c0002t0001g0135a0001c0002t0001g0136others(12): Show | 16 | HG01109.hp1 HG01516.hp2 HG01993.hp2 others(13): Show |
intron_variant | MODIFIER | c.651-1406G>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 6/8 | chr15 | 59512883 | ||||||
| chr15:59512886
|
G | A | 1 | a0001c0001t0001g0102 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.651-1403G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 6/8 | chr15 | 59512886 | ||||||
| chr15:59512916
|
A | T | 1 | a0001c0001t0001g0192 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.651-1373A>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 6/8 | chr15 | 59512916 | ||||||
| chr15:59512992
|
A | G | 15 | a0001c0002t0001g0056a0001c0002t0001g0135a0001c0002t0001g0136others(12): Show | 16 | HG01109.hp1 HG01516.hp2 HG01993.hp2 others(13): Show |
intron_variant | MODIFIER | c.651-1297A>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 6/8 | chr15 | 59512992 | ||||||
| chr15:59513062
|
C | T | 6 | a0001c0002t0002g0050a0001c0002t0002g0145a0001c0003t0002g0004others(3): Show | 7 | HG02622.hp1 HG02630.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.651-1227C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 6/8 | chr15 | 59513062 | ||||||
| chr15:59513076
|
A | G | 2 | a0001c0002t0001g0350a0001c0002t0013g0239 | 2 | HG02615.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.651-1213A>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 6/8 | chr15 | 59513076 | ||||||
| chr15:59513301
|
G | A | 11 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0016others(8): Show | 13 | HG00735.hp1 HG00741.hp2 HG01074.hp2 others(10): Show |
intron_variant | MODIFIER | c.651-988G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 6/8 | chr15 | 59513301 | ||||||
| chr15:59513416
|
G | A | 1 | a0001c0001t0001g0073 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.651-873G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 6/8 | chr15 | 59513416 | ||||||
| chr15:59513491
|
T | C | 1 | a0001c0001t0001g0303 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.651-798T>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 6/8 | chr15 | 59513491 | ||||||
| chr15:59513637
|
A | T | 1 | a0001c0002t0012g0146 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.651-652A>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 6/8 | chr15 | 59513637 | ||||||
| chr15:59513717
|
C | T | 4 | a0001c0001t0001g0240a0001c0001t0001g0241a0001c0001t0001g0337others(1): Show | 4 | HG02818.hp1 HG03209.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.651-572C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 6/8 | chr15 | 59513717 | ||||||
| chr15:59513794
|
G | C | 3 | a0001c0002t0001g0135a0001c0002t0001g0136a0001c0002t0012g0146 | 3 | HG02895.hp1 HG02897.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.651-495G>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 6/8 | chr15 | 59513794 | ||||||
| chr15:59514085
|
G | T | 209 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(206): Show | 212 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(209): Show |
intron_variant | MODIFIER | c.651-204G>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 6/8 | chr15 | 59514085 | ||||||
| chr15:59514113
|
C | G | 1 | a0004c0008t0001g0309 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.651-176C>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 6/8 | chr15 | 59514113 | ||||||
| chr15:59514470
|
G | A | 3 | a0001c0002t0001g0135a0001c0002t0001g0136a0001c0002t0012g0146 | 3 | HG02895.hp1 HG02897.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.786+46G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 7/8 | chr15 | 59514470 | ||||||
| chr15:59514490
|
A | G | 2 | a0001c0001t0001g0226a0001c0002t0001g0224 | 2 | HG02280.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.786+66A>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 7/8 | chr15 | 59514490 | ||||||
| chr15:59514518
|
A | G | 4 | a0001c0003t0002g0004a0001c0003t0002g0051a0001c0003t0002g0052others(1): Show | 5 | HG02622.hp1 HG02630.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.786+94A>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 7/8 | chr15 | 59514518 | ||||||
| chr15:59514878
|
T | C | 3 | a0001c0002t0003g0139a0001c0002t0012g0146a0001c0002t0014g0140 | 3 | HG02451.hp2 HG03225.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.786+454T>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 7/8 | chr15 | 59514878 | ||||||
| chr15:59514879
|
C | T | 1 | a0001c0001t0001g0064 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.786+455C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 7/8 | chr15 | 59514879 | ||||||
| chr15:59514902
|
C | G | 2 | a0001c0002t0004g0015a0001c0002t0011g0010 | 3 | HG02647.hp1 HG02970.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.786+478C>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 7/8 | chr15 | 59514902 | ||||||
| chr15:59515026
|
C | G | 83 | a0001c0001t0001g0083a0001c0001t0001g0120a0001c0001t0001g0129others(80): Show | 83 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.786+602C>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 7/8 | chr15 | 59515026 | ||||||
| chr15:59515155
|
T | G | 13 | a0001c0002t0003g0139a0001c0002t0003g0141a0001c0002t0003g0142others(10): Show | 13 | HG01884.hp2 HG02451.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.786+731T>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 7/8 | chr15 | 59515155 | ||||||
| chr15:59515350
|
T | C | 13 | a0001c0002t0003g0139a0001c0002t0003g0141a0001c0002t0003g0142others(10): Show | 13 | HG01884.hp2 HG02451.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.786+926T>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 7/8 | chr15 | 59515350 | ||||||
| chr15:59515374
|
G | A | 13 | a0001c0002t0003g0139a0001c0002t0003g0141a0001c0002t0003g0142others(10): Show | 13 | HG01884.hp2 HG02451.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.786+950G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 7/8 | chr15 | 59515374 | ||||||
| chr15:59515633
|
A | G | 1 | a0001c0002t0001g0053 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.787-1012A>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 7/8 | chr15 | 59515633 | ||||||
| chr15:59515641
|
T | A | 1 | a0001c0002t0001g0041 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.787-1004T>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 7/8 | chr15 | 59515641 | ||||||
| chr15:59515743
|
C | T | 1 | a0001c0001t0001g0250 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.787-902C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 7/8 | chr15 | 59515743 | ||||||
| chr15:59515744
|
T | C | 1 | a0001c0001t0001g0250 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.787-901T>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 7/8 | chr15 | 59515744 | ||||||
| chr15:59515746
|
A | C | 1 | a0001c0001t0001g0250 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.787-899A>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 7/8 | chr15 | 59515746 | ||||||
| chr15:59515748
|
A | G | 1 | a0001c0001t0001g0250 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.787-897A>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 7/8 | chr15 | 59515748 | ||||||
| chr15:59515749
|
A | T | 1 | a0001c0001t0001g0250 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.787-896A>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 7/8 | chr15 | 59515749 | ||||||
| chr15:59515752
|
C | T | 1 | a0001c0001t0001g0250 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.787-893C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 7/8 | chr15 | 59515752 | ||||||
| chr15:59515754
|
T | A | 1 | a0001c0001t0001g0250 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.787-891T>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 7/8 | chr15 | 59515754 | ||||||
| chr15:59515755
|
G | T | 1 | a0001c0001t0001g0250 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.787-890G>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 7/8 | chr15 | 59515755 | ||||||
| chr15:59515756
|
G | T | 1 | a0001c0001t0001g0250 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.787-889G>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 7/8 | chr15 | 59515756 | ||||||
| chr15:59515758
|
C | T | 1 | a0001c0001t0001g0250 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.787-887C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 7/8 | chr15 | 59515758 | ||||||
| chr15:59515759
|
T | A | 1 | a0001c0001t0001g0250 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.787-886T>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 7/8 | chr15 | 59515759 | ||||||
| chr15:59515761
|
T | A | 1 | a0001c0001t0001g0250 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.787-884T>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 7/8 | chr15 | 59515761 | ||||||
| chr15:59516012
|
T | A | 11 | a0001c0002t0001g0056a0001c0002t0004g0015a0001c0002t0004g0244others(8): Show | 12 | HG01109.hp1 HG01516.hp2 HG01993.hp2 others(9): Show |
intron_variant | MODIFIER | c.787-633T>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 7/8 | chr15 | 59516012 | ||||||
| chr15:59516126
|
G | GT | 26 | a0001c0001t0001g0057a0001c0001t0001g0079a0001c0001t0001g0101others(23): Show | 26 | HG00642.hp2 HG00741.hp1 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.787-501dupT | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr15 | 59516126 | |||||
| chr15:59516126
|
G | T | 1 | a0001c0001t0001g0268 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.787-519G>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 7/8 | chr15 | 59516126 | ||||||
| chr15:59516175
|
G | A | 9 | a0001c0001t0001g0063a0001c0001t0001g0091a0001c0001t0001g0092others(6): Show | 9 | HG01069.hp1 HG01071.hp2 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.787-470G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 7/8 | chr15 | 59516175 | ||||||
| chr15:59516323
|
T | C | 2 | a0001c0001t0001g0134a0001c0001t0001g0137 | 2 | HG02109.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.787-322T>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 7/8 | chr15 | 59516323 | ||||||
| chr15:59516327
|
A | T | 3 | a0001c0001t0001g0109a0001c0001t0001g0200a0001c0001t0001g0214 | 3 | NA18944.hp1 NA19010.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.787-318A>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 7/8 | chr15 | 59516327 | ||||||
| chr15:59516343
|
T | C | 1 | a0001c0002t0008g0255 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.787-302T>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 7/8 | chr15 | 59516343 | ||||||
| chr15:59516381
|
C | T | 4 | a0001c0001t0001g0336a0001c0001t0001g0338a0001c0002t0001g0135others(1): Show | 4 | HG02055.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.787-264C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 7/8 | chr15 | 59516381 | ||||||
| chr15:59517030
|
A | G | 1 | a0001c0001t0001g0351 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.982+190A>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 8/8 | chr15 | 59517030 | ||||||
| chr15:59517083
|
C | T | 3 | a0001c0003t0002g0004a0001c0003t0002g0051a0001c0003t0002g0052 | 4 | HG02622.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.982+243C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 8/8 | chr15 | 59517083 | ||||||
| chr15:59517358
|
C | G | 11 | a0001c0002t0003g0139a0001c0002t0003g0141a0001c0002t0003g0142others(8): Show | 11 | HG01884.hp2 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.982+518C>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 8/8 | chr15 | 59517358 | ||||||
| chr15:59517420
|
G | T | 11 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0016others(8): Show | 13 | HG00735.hp1 HG00741.hp2 HG01074.hp2 others(10): Show |
intron_variant | MODIFIER | c.982+580G>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 8/8 | chr15 | 59517420 | ||||||
| chr15:59517431
|
A | T | 7 | a0001c0001t0001g0044a0001c0001t0001g0062a0001c0001t0001g0070others(4): Show | 7 | HG00673.hp1 HG02056.hp2 NA18962.hp2 others(4): Show |
intron_variant | MODIFIER | c.982+591A>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 8/8 | chr15 | 59517431 | ||||||
| chr15:59517455
|
A | C | 12 | a0001c0001t0001g0077a0001c0001t0001g0149a0001c0001t0001g0158others(9): Show | 12 | HG01243.hp1 HG01256.hp1 HG02132.hp1 others(9): Show |
intron_variant | MODIFIER | c.982+615A>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 8/8 | chr15 | 59517455 | ||||||
| chr15:59517515
|
G | C | 11 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0016others(8): Show | 13 | HG00735.hp1 HG00741.hp2 HG01074.hp2 others(10): Show |
intron_variant | MODIFIER | c.982+675G>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 8/8 | chr15 | 59517515 | ||||||
| chr15:59517586
|
C | A | 1 | a0001c0001t0001g0083 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.982+746C>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 8/8 | chr15 | 59517586 | ||||||
| chr15:59517727
|
A | G | 3 | a0001c0001t0001g0286a0001c0001t0001g0363a0001c0001t0019g0223 | 3 | HG02965.hp1 HG03579.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.982+887A>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 8/8 | chr15 | 59517727 | ||||||
| chr15:59517878
|
G | A | 13 | a0001c0002t0003g0139a0001c0002t0003g0141a0001c0002t0003g0142others(10): Show | 13 | HG01884.hp2 HG02451.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.982+1038G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 8/8 | chr15 | 59517878 | ||||||
| chr15:59517892
|
C | T | 1 | a0001c0002t0001g0330 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.982+1052C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 8/8 | chr15 | 59517892 | ||||||
| chr15:59517899
|
T | C | 1 | a0001c0002t0001g0053 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.982+1059T>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 8/8 | chr15 | 59517899 | ||||||
| chr15:59517945
|
A | G | 2 | a0001c0002t0010g0257a0001c0002t0010g0258 | 2 | HG03098.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.982+1105A>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 8/8 | chr15 | 59517945 | ||||||
| chr15:59517973
|
C | CT | 12 | a0001c0001t0001g0060a0001c0001t0001g0066a0001c0001t0001g0090others(9): Show | 13 | HG00733.hp2 HG00741.hp1 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.982+1145dupT | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr15 | 59517973 | |||||
| chr15:59518014
|
C | A | 3 | a0001c0002t0010g0257a0001c0002t0010g0258a0001c0002t0012g0146 | 3 | HG03098.hp1 HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.982+1174C>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 8/8 | chr15 | 59518014 | ||||||
| chr15:59518070
|
A | T | 40 | a0001c0001t0001g0144a0001c0002t0001g0011a0001c0002t0001g0350others(37): Show | 42 | HG01109.hp1 HG01516.hp2 HG01884.hp2 others(39): Show |
intron_variant | MODIFIER | c.982+1230A>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 8/8 | chr15 | 59518070 | ||||||
| chr15:59518113
|
C | T | 2 | a0001c0001t0001g0286a0001c0001t0001g0363 | 2 | HG02965.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.982+1273C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 8/8 | chr15 | 59518113 | ||||||
| chr15:59518117
|
C | T | 1 | a0001c0002t0012g0146 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.982+1277C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 8/8 | chr15 | 59518117 | ||||||
| chr15:59518139
|
A | AT | 32 | a0001c0001t0001g0027a0001c0001t0001g0154a0001c0001t0001g0181others(29): Show | 33 | HG00673.hp2 HG00738.hp1 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.982+1317dupT | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr15 | 59518139 | |||||
| chr15:59518139
|
AT | A | 12 | a0001c0001t0001g0103a0001c0001t0001g0201a0001c0001t0001g0202others(9): Show | 12 | HG01169.hp1 HG01257.hp1 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.982+1317delT | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr15 | 59518139 | |||||
| chr15:59518309
|
C | A | 1 | a0002c0004t0004g0253 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.982+1469C>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 8/8 | chr15 | 59518309 | ||||||
| chr15:59518365
|
C | G | 122 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(119): Show | 127 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.982+1525C>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 8/8 | chr15 | 59518365 | ||||||
| chr15:59518391
|
G | A | 1 | a0001c0002t0013g0239 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.982+1551G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 8/8 | chr15 | 59518391 | ||||||
| chr15:59518432
|
C | T | 1 | a0001c0001t0001g0221 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.982+1592C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 8/8 | chr15 | 59518432 | ||||||
| chr15:59518733
|
C | T | 5 | a0001c0001t0001g0074a0001c0001t0001g0080a0001c0001t0001g0110others(2): Show | 5 | NA18959.hp2 NA18983.hp2 NA19007.hp2 others(2): Show |
intron_variant | MODIFIER | c.982+1893C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 8/8 | chr15 | 59518733 | ||||||
| chr15:59518759
|
C | G | 1 | a0001c0001t0001g0361 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.982+1919C>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 8/8 | chr15 | 59518759 | ||||||
| chr15:59518777
|
C | A | 1 | a0001c0002t0002g0145 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.982+1937C>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 8/8 | chr15 | 59518777 | ||||||
| chr15:59518806
|
A | C | 100 | a0001c0001t0001g0063a0001c0001t0001g0083a0001c0001t0001g0091others(97): Show | 100 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.982+1966A>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 8/8 | chr15 | 59518806 | ||||||
| chr15:59518853
|
T | C | 1 | a0001c0002t0001g0350 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.982+2013T>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 8/8 | chr15 | 59518853 | ||||||
| chr15:59518906
|
CAT | C | 3 | a0001c0001t0001g0286a0001c0001t0001g0363a0001c0001t0019g0223 | 3 | HG02965.hp1 HG03579.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.982+2069_982+2070d others(4): Show |
FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr15 | 59518906 | |||||
| chr15:59518943
|
C | CTG | 124 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(121): Show | 130 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.982+2136_982+2137d others(4): Show |
FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr15 | 59518943 | |||||
| chr15:59518943
|
C | CTGTG | 9 | a0001c0001t0001g0090a0001c0001t0001g0104a0001c0001t0001g0108others(6): Show | 9 | HG00733.hp2 HG01243.hp1 HG01261.hp2 others(6): Show |
intron_variant | MODIFIER | c.982+2134_982+2137d others(6): Show |
FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr15 | 59518943 | |||||
| chr15:59518943
|
C | G | 1 | a0001c0002t0001g0011 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.982+2103C>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 8/8 | chr15 | 59518943 | ||||||
| chr15:59518943
|
CTG | C | 24 | a0001c0001t0001g0062a0001c0001t0001g0076a0001c0001t0001g0149others(21): Show | 24 | HG01243.hp2 HG01256.hp1 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.982+2136_982+2137d others(4): Show |
FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr15 | 59518943 | |||||
| chr15:59518943
|
CTGTG | C | 8 | a0001c0001t0001g0153a0001c0001t0001g0181a0001c0001t0001g0219others(5): Show | 9 | HG00738.hp1 HG02145.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.982+2134_982+2137d others(6): Show |
FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr15 | 59518943 | |||||
| chr15:59518943
|
CTGTGTGT others(3): Show |
C | 8 | a0001c0002t0001g0350a0001c0002t0004g0244a0001c0002t0004g0246others(5): Show | 8 | HG01109.hp1 HG01516.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.982+2128_982+2137d others(12): Show |
FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr15 | 59518943 | |||||
| chr15:59519242
|
G | A | 2 | a0001c0001t0001g0085a0001c0001t0001g0086 | 2 | NA18943.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.983-2012G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 8/8 | chr15 | 59519242 | ||||||
| chr15:59519267
|
C | T | 1 | a0001c0001t0001g0196 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.983-1987C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 8/8 | chr15 | 59519267 | ||||||
| chr15:59519316
|
G | T | 5 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0355others(2): Show | 5 | HG02818.hp2 HG02976.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.983-1938G>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 8/8 | chr15 | 59519316 | ||||||
| chr15:59519409
|
A | G | 40 | a0001c0001t0001g0144a0001c0002t0001g0011a0001c0002t0001g0350others(37): Show | 42 | HG01109.hp1 HG01516.hp2 HG01884.hp2 others(39): Show |
intron_variant | MODIFIER | c.983-1845A>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 8/8 | chr15 | 59519409 | ||||||
| chr15:59519472
|
T | C | 14 | a0001c0002t0003g0139a0001c0002t0003g0141a0001c0002t0003g0142others(11): Show | 14 | HG01884.hp2 HG02451.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.983-1782T>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 8/8 | chr15 | 59519472 | ||||||
| chr15:59519512
|
C | T | 1 | a0001c0002t0003g0143 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.983-1742C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 8/8 | chr15 | 59519512 | ||||||
| chr15:59519580
|
C | T | 6 | a0001c0002t0002g0050a0001c0002t0002g0145a0001c0003t0002g0004others(3): Show | 7 | HG02622.hp1 HG02630.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.983-1674C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 8/8 | chr15 | 59519580 | ||||||
| chr15:59519583
|
C | T | 1 | a0001c0002t0001g0041 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.983-1671C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 8/8 | chr15 | 59519583 | ||||||
| chr15:59519631
|
T | A | 14 | a0001c0002t0003g0139a0001c0002t0003g0141a0001c0002t0003g0142others(11): Show | 14 | HG01884.hp2 HG02451.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.983-1623T>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 8/8 | chr15 | 59519631 | ||||||
| chr15:59519776
|
T | C | 2 | a0001c0002t0001g0024a0001c0002t0001g0260 | 2 | NA18977.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.983-1478T>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 8/8 | chr15 | 59519776 | ||||||
| chr15:59519940
|
C | T | 1 | a0001c0002t0001g0350 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.983-1314C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 8/8 | chr15 | 59519940 | ||||||
| chr15:59519950
|
T | A | 2 | a0001c0001t0001g0152a0001c0001t0001g0153 | 2 | HG02723.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.983-1304T>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 8/8 | chr15 | 59519950 | ||||||
| chr15:59519952
|
G | A | 2 | a0001c0001t0001g0152a0001c0001t0001g0153 | 2 | HG02723.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.983-1302G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 8/8 | chr15 | 59519952 | ||||||
| chr15:59520099
|
A | AT | 305 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(302): Show | 313 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(310): Show |
intron_variant | MODIFIER | c.983-1144dupT | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr15 | 59520099 | |||||
| chr15:59520163
|
A | G | 12 | a0001c0002t0004g0015a0001c0002t0004g0244a0001c0002t0004g0246others(9): Show | 13 | HG01109.hp1 HG01516.hp2 HG02647.hp1 others(10): Show |
intron_variant | MODIFIER | c.983-1091A>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 8/8 | chr15 | 59520163 | ||||||
| chr15:59520189
|
T | C | 34 | a0001c0002t0001g0011a0001c0002t0001g0350a0001c0002t0002g0050others(31): Show | 36 | HG01109.hp1 HG01516.hp2 HG01884.hp2 others(33): Show |
intron_variant | MODIFIER | c.983-1065T>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 8/8 | chr15 | 59520189 | ||||||
| chr15:59520298
|
C | A | 1 | a0001c0002t0001g0029 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.983-956C>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 8/8 | chr15 | 59520298 | ||||||
| chr15:59520307
|
G | A | 7 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0351others(4): Show | 7 | HG00733.hp1 HG01168.hp2 HG01261.hp1 others(4): Show |
intron_variant | MODIFIER | c.983-947G>A | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 8/8 | chr15 | 59520307 | ||||||
| chr15:59520374
|
A | G | 2 | a0001c0002t0010g0257a0001c0002t0010g0258 | 2 | HG03098.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.983-880A>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 8/8 | chr15 | 59520374 | ||||||
| chr15:59520392
|
G | T | 3 | a0001c0001t0001g0071a0001c0001t0001g0198a0001c0001t0001g0272 | 3 | HG02056.hp1 HG02071.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.983-862G>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 8/8 | chr15 | 59520392 | ||||||
| chr15:59520435
|
T | G | 2 | a0001c0001t0001g0250a0001c0001t0001g0251 | 2 | NA18952.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.983-819T>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 8/8 | chr15 | 59520435 | ||||||
| chr15:59520535
|
C | G | 2 | a0001c0001t0001g0057a0001c0001t0001g0131 | 2 | HG02155.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.983-719C>G | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 8/8 | chr15 | 59520535 | ||||||
| chr15:59520558
|
G | C | 6 | a0001c0002t0002g0050a0001c0002t0002g0145a0001c0003t0002g0004others(3): Show | 7 | HG02622.hp1 HG02630.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.983-696G>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 8/8 | chr15 | 59520558 | ||||||
| chr15:59520563
|
A | AT | 7 | a0001c0001t0001g0259a0001c0001t0001g0269a0001c0001t0001g0302others(4): Show | 7 | HG01515.hp2 HG01517.hp2 HG02698.hp2 others(4): Show |
intron_variant | MODIFIER | c.983-672dupT | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr15 | 59520563 | |||||
| chr15:59520563
|
AT | A | 125 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(122): Show | 130 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.983-672delT | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr15 | 59520563 | |||||
| chr15:59520764
|
C | T | 1 | a0001c0002t0012g0146 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.983-490C>T | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 8/8 | chr15 | 59520764 | ||||||
| chr15:59520892
|
T | C | 1 | a0001c0002t0001g0011 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.983-362T>C | FAM81A | ENSG00000157470.12 | transcript | ENST00000288228.10 | protein_coding | 8/8 | chr15 | 59520892 |